Canonical Allele Identifier: CA481331558
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103246697A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102852919A>C , CM000674.2:g.102852919A>C GRCh38
NC_000012.11:g.103246697A>C , CM000674.1:g.103246697A>C GRCh37
NC_000012.10:g.101770827A>C NCBI36
NG_008690.1:g.69684T>G
NG_008690.2:g.110492T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.738T>G MANE Select ENSP00000448059.1:p.Ala246=
ENST00000307000.7:c.723T>G ENSP00000303500.2:p.Ala241=
ENST00000549247.6:n.497T>G
ENST00000553106.5:c.738T>G ENSP00000448059.1:p.Ala246=
NM_000277.1:c.738T>G NP_000268.1:p.Ala246=
XM_011538422.1:c.738T>G XP_011536724.1:p.Ala246=
NM_000277.2:c.738T>G NP_000268.1:p.Ala246=
NM_001354304.1:c.738T>G NP_001341233.1:p.Ala246=
NM_000277.3:c.738T>G MANE Select NP_000268.1:p.Ala246=
NM_001354304.2:c.738T>G NP_001341233.1:p.Ala246=