Canonical Allele Identifier: CA386296858
Gene: PAH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102855283A>C , CM000674.2:g.102855283A>C GRCh38
NC_000012.11:g.103249061A>C , CM000674.1:g.103249061A>C GRCh37
NC_000012.10:g.101773191A>C NCBI36
NG_008690.1:g.67320T>G
NG_008690.2:g.108128T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.559T>G MANE Select ENSP00000448059.1:p.Trp187Gly
ENST00000307000.7:c.544T>G ENSP00000303500.2:p.Trp182Gly
ENST00000549111.5:n.655T>G
ENST00000551988.5:n.580T>G
ENST00000553106.5:c.559T>G ENSP00000448059.1:p.Trp187Gly
NM_000277.1:c.559T>G NP_000268.1:p.Trp187Gly
XM_011538422.1:c.559T>G XP_011536724.1:p.Trp187Gly
NM_000277.2:c.559T>G NP_000268.1:p.Trp187Gly
NM_001354304.1:c.559T>G NP_001341233.1:p.Trp187Gly
XM_017019370.2:c.559T>G XP_016874859.1:p.Trp187Gly
NM_000277.3:c.559T>G MANE Select NP_000268.1:p.Trp187Gly
NM_001354304.2:c.559T>G NP_001341233.1:p.Trp187Gly