Canonical Allele Identifier: CA481375357
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103234230A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840452A>G , CM000674.2:g.102840452A>G GRCh38
NC_000012.11:g.103234230A>G , CM000674.1:g.103234230A>G GRCh37
NC_000012.10:g.101758360A>G NCBI36
NG_008690.1:g.82151T>C
NG_008690.2:g.122959T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1263T>C MANE Select ENSP00000448059.1:p.Ile421=
ENST00000307000.7:c.1248T>C ENSP00000303500.2:p.Ile416=
ENST00000551114.2:n.925T>C
ENST00000553106.5:c.1263T>C ENSP00000448059.1:p.Ile421=
ENST00000635477.1:c.367T>C
ENST00000635528.1:n.778T>C
NM_000277.1:c.1263T>C NP_000268.1:p.Ile421=
XM_011538422.1:c.1206T>C XP_011536724.1:p.Ile402=
NM_000277.2:c.1263T>C NP_000268.1:p.Ile421=
NM_001354304.1:c.1263T>C NP_001341233.1:p.Ile421=
NM_000277.3:c.1263T>C MANE Select NP_000268.1:p.Ile421=
NM_001354304.2:c.1263T>C NP_001341233.1:p.Ile421=