Canonical Allele Identifier: CA2560809490
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102865735_102865736insTAGTCAGCAAT , CM000674.2:g.102865735_102865736insTAGTCAGCAAT GRCh38
NC_000012.11:g.103259513_103259514insTAGTCAGCAAT , CM000674.1:g.103259513_103259514insTAGTCAGCAAT GRCh37
NC_000012.10:g.101783643_101783644insTAGTCAGCAAT NCBI36
NG_008690.1:g.56867_56868insATTGCTGACTA
NG_008690.2:g.97675_97676insATTGCTGACTA

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.509+860_509+861insATTGCTGACTA MANE Select ENSP00000448059.1:n.509+860_509+861insATT...
ENST00000307000.7:c.494+860_494+861insATTGCTGACTA ENSP00000303500.2:n.494+860_494+861insATT...
ENST00000549111.5:n.605+860_605+861insATTGCTGACTA
ENST00000551988.5:n.531-10404_531-10403insATTGCTGACTA
ENST00000553106.5:c.509+860_509+861insATTGCTGACTA ENSP00000448059.1:n.509+860_509+861insATT...
NM_000277.1:c.509+860_509+861insATTGCTGACTA NP_000268.1:n.509+860_509+861insATTGCTGAC...
XM_011538422.1:c.509+860_509+861insATTGCTGACTA XP_011536724.1:n.509+860_509+861insATTGCT...
NM_000277.2:c.509+860_509+861insATTGCTGACTA NP_000268.1:n.509+860_509+861insATTGCTGAC...
NM_001354304.1:c.509+860_509+861insATTGCTGACTA NP_001341233.1:n.509+860_509+861insATTGCT...
XM_017019370.2:c.509+860_509+861insATTGCTGACTA XP_016874859.1:n.509+860_509+861insATTGCT...
NM_000277.3:c.509+860_509+861insATTGCTGACTA MANE Select NP_000268.1:n.509+860_509+861insATTGCTGAC...
NM_001354304.2:c.509+860_509+861insATTGCTGACTA NP_001341233.1:n.509+860_509+861insATTGCT...