Allele Registry

HGVS	Genome Assembly
NC_000005.10:g.156508647_156508650delinsAAGG , CM000667.2:g.156508647_156508650delinsAAGG	GRCh38
NC_000005.9:g.155935657_155935660delinsAAGG , CM000667.1:g.155935657_155935660delinsAAGG	GRCh37
NC_000005.8:g.155868235_155868238delinsAAGG	NCBI36
NG_008693.2:g.643304_643307delinsAAGG , LRG_205:g.643304_643307delinsAAGG

HGVS	Amino-acid Change
ENST00000337851.9:c.239_242delinsAAGG MANE Select	ENSP00000338343.4:p.Glu80=
ENST00000337851.8:c.239_242delinsAAGG	ENSP00000338343.4:p.Glu80=
ENST00000435422.7:c.236_239delinsAAGG	ENSP00000403003.2:p.Glu79=
ENST00000517913.5:c.239_242delinsAAGG	ENSP00000429378.1:p.Glu80=
ENST00000524347.2:c.103_106delinsAAGG	ENSP00000430794.1:n.103_106delinsAAGG
NM_000337.5:c.239_242delinsAAGG , LRG_205t1:c.239_242delinsAAGG	NP_000328.2:p.Glu80=
NM_001128209.1:c.236_239delinsAAGG	NP_001121681.1:p.Glu79=
NM_172244.2:c.239_242delinsAAGG	NP_758447.1:p.Glu80=
XM_005265966.3:c.239_242delinsAAGG	XP_005266023.1:p.Glu80=
XM_005265967.1:c.239_242delinsAAGG	XP_005266024.1:p.Glu80=
XM_006714911.2:c.239_242delinsAAGG	XP_006714974.1:p.Glu80=
XM_011534621.1:c.236_239delinsAAGG	XP_011532923.1:p.Glu79=
XM_005265966.5:c.239_242delinsAAGG	XP_005266023.1:p.Glu80=
XM_005265967.2:c.239_242delinsAAGG	XP_005266024.1:p.Glu80=
XM_011534621.2:c.236_239delinsAAGG	XP_011532923.1:p.Glu79=
XM_017009723.2:c.239_242delinsAAGG	XP_016865212.1:p.Glu80=
XM_017009724.1:c.239_242delinsAAGG	XP_016865213.1:p.Glu80=
NM_001128209.2:c.236_239delinsAAGG	NP_001121681.1:p.Glu79=
NM_172244.3:c.239_242delinsAAGG	NP_758447.1:p.Glu80=
NM_000337.6:c.239_242delinsAAGG MANE Select	NP_000328.2:p.Glu80=