Canonical Allele Identifier: CA242744377
Gene: PAH HGNC NCBI

Linked Data

dbSNP Id: rs200380893

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102844181_102844182insCG , CM000674.2:g.102844181_102844182insCG GRCh38
NC_000012.11:g.103237959_103237960insCG , CM000674.1:g.103237959_103237960insCG GRCh37
NC_000012.10:g.101762089_101762090insCG NCBI36
NG_008690.1:g.78421_78422insCG
NG_008690.2:g.119229_119230insCG

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1065+154_1065+155insCG MANE Select ENSP00000448059.1:n.1065+154_1065+155insC...
ENST00000307000.7:c.1050+154_1050+155insCG ENSP00000303500.2:n.1050+154_1050+155insC...
ENST00000549247.6:n.824+154_824+155insCG
ENST00000551114.2:n.727+154_727+155insCG
ENST00000553106.5:c.1065+154_1065+155insCG ENSP00000448059.1:n.1065+154_1065+155insC...
ENST00000635477.1:c.169+154_169+155insCG
ENST00000635528.1:n.580+154_580+155insCG
NM_000277.1:c.1065+154_1065+155insCG NP_000268.1:n.1065+154_1065+155insCG
XM_011538422.1:c.1008+154_1008+155insCG XP_011536724.1:n.1008+154_1008+155insCG
NM_000277.2:c.1065+154_1065+155insCG NP_000268.1:n.1065+154_1065+155insCG
NM_001354304.1:c.1065+154_1065+155insCG NP_001341233.1:n.1065+154_1065+155insCG
NM_000277.3:c.1065+154_1065+155insCG MANE Select NP_000268.1:n.1065+154_1065+155insCG
NM_001354304.2:c.1065+154_1065+155insCG NP_001341233.1:n.1065+154_1065+155insCG