Canonical Allele Identifier: CA2726966278
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs2136631677

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840237dup , CM000674.2:g.102840237dup GRCh38
NC_000012.11:g.103234015dup , CM000674.1:g.103234015dup GRCh37
NC_000012.10:g.101758145dup NCBI36
NG_008690.1:g.82366dup
NG_008690.2:g.123174dup

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1315+163dup MANE Select ENSP00000448059.1:n.1315+163dup
ENST00000307000.7:c.1300+163dup ENSP00000303500.2:n.1300+163dup
ENST00000551114.2:n.977+163dup
ENST00000553106.5:c.1315+163dup ENSP00000448059.1:n.1315+163dup
ENST00000635477.1:c.419+163dup
ENST00000635528.1:n.830+163dup
NM_000277.1:c.1315+163dup NP_000268.1:n.1315+163dup
XM_011538422.1:c.1258+163dup XP_011536724.1:n.1258+163dup
NM_000277.2:c.1315+163dup NP_000268.1:n.1315+163dup
NM_001354304.1:c.1315+163dup NP_001341233.1:n.1315+163dup
NM_000277.3:c.1315+163dup MANE Select NP_000268.1:n.1315+163dup
NM_001354304.2:c.1315+163dup NP_001341233.1:n.1315+163dup