Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11100257_11100280delinsCCAAGACGGGAAATGCATCTCCTA , CM000681.2:g.11100257_11100280delinsCCAAGACGGGAAATGCATCTCCTA	GRCh38
NC_000019.9:g.11210933_11210956delinsCCAAGACGGGAAATGCATCTCCTA , CM000681.1:g.11210933_11210956delinsCCAAGACGGGAAATGCATCTCCTA	GRCh37
NC_000019.8:g.11071933_11071956delinsCCAAGACGGGAAATGCATCTCCTA	NCBI36
NG_009060.1:g.15877_15900delinsCCAAGACGGGAAATGCATCTCCTA , LRG_274:g.15877_15900delinsCCAAGACGGGAAATGCATCTCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.360_383delinsCCAAGACGGGAAATGCATCTCCTA	ENSP00000252444.6:p.Cys120=
ENST00000559340.2:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	ENSP00000453696.2:p.Cys34=
ENST00000560467.2:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	ENSP00000453513.2:p.Cys34=
ENST00000558518.6:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA MANE Select	ENSP00000454071.1:p.Cys34=
ENST00000252444.9:c.356_379delinsCCAAGACGGGAAATGCATCTCCTA
ENST00000455727.6:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	ENSP00000397829.2:p.Cys34=
ENST00000535915.5:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	ENSP00000440520.1:p.Cys34=
ENST00000545707.5:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	ENSP00000437639.1:p.Cys34=
ENST00000557933.5:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	ENSP00000453557.1:p.Cys34=
ENST00000557958.1:n.188_211delinsCCAAGACGGGAAATGCATCTCCTA
ENST00000558013.5:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	ENSP00000453346.1:p.Cys34=
ENST00000558518.5:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	ENSP00000454071.1:p.Cys34=
ENST00000560502.5:n.188_211delinsCCAAGACGGGAAATGCATCTCCTA
NM_000527.4:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA , LRG_274t1:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	NP_000518.1:p.Cys34=
NM_001195798.1:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	NP_001182727.1:p.Cys34=
NM_001195799.1:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	NP_001182728.1:p.Cys34=
NM_001195800.1:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	NP_001182729.1:p.Cys34=
NM_001195803.1:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	NP_001182732.1:p.Cys34=
XM_011528010.1:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	XP_011526312.1:p.Cys34=
XM_011528011.1:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	XP_011526313.1:p.Cys34=
XR_244074.2:n.252_275delinsCCAAGACGGGAAATGCATCTCCTA
XM_011528010.2:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	XP_011526312.1:p.Cys34=
XR_001753685.2:n.219_242delinsCCAAGACGGGAAATGCATCTCCTA
XR_001753686.2:n.219_242delinsCCAAGACGGGAAATGCATCTCCTA
NM_000527.5:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA MANE Select	NP_000518.1:p.Cys34=
NM_001195798.2:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	NP_001182727.1:p.Cys34=
NM_001195799.2:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	NP_001182728.1:p.Cys34=
NM_001195800.2:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	NP_001182729.1:p.Cys34=
NM_001195803.2:c.102_125delinsCCAAGACGGGAAATGCATCTCCTA	NP_001182732.1:p.Cys34=