Canonical Allele Identifier: CA2059447612
Gene: PAH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844156_102844157delinsCT , CM000674.2:g.102844156_102844157delinsCT GRCh38
NC_000012.11:g.103237934_103237935delinsCT , CM000674.1:g.103237934_103237935delinsCT GRCh37
NC_000012.10:g.101762064_101762065delinsCT NCBI36
NG_008690.1:g.78446_78447delinsAG
NG_008690.2:g.119254_119255delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1065+179_1065+180delinsAG MANE Select ENSP00000448059.1:n.1065+179_1065+180deli...
ENST00000307000.7:c.1050+179_1050+180delinsAG ENSP00000303500.2:n.1050+179_1050+180deli...
ENST00000549247.6:n.824+179_824+180delinsAG
ENST00000551114.2:n.727+179_727+180delinsAG
ENST00000553106.5:c.1065+179_1065+180delinsAG ENSP00000448059.1:n.1065+179_1065+180deli...
ENST00000635477.1:c.169+179_169+180delinsAG
ENST00000635528.1:n.580+179_580+180delinsAG
NM_000277.1:c.1065+179_1065+180delinsAG NP_000268.1:n.1065+179_1065+180delinsAG
XM_011538422.1:c.1008+179_1008+180delinsAG XP_011536724.1:n.1008+179_1008+180delinsA...
NM_000277.2:c.1065+179_1065+180delinsAG NP_000268.1:n.1065+179_1065+180delinsAG
NM_001354304.1:c.1065+179_1065+180delinsAG NP_001341233.1:n.1065+179_1065+180delinsA...
NM_000277.3:c.1065+179_1065+180delinsAG MANE Select NP_000268.1:n.1065+179_1065+180delinsAG
NM_001354304.2:c.1065+179_1065+180delinsAG NP_001341233.1:n.1065+179_1065+180delinsA...