Canonical Allele Identifier: CA386302333
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103306592C>A (hg19) chr12:g.102912814C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102912814C>A , CM000674.2:g.102912814C>A GRCh38
NC_000012.11:g.103306592C>A , CM000674.1:g.103306592C>A GRCh37
NC_000012.10:g.101830722C>A NCBI36
NG_008690.1:g.9789G>T
NG_008690.2:g.50597G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.145G>T MANE Select ENSP00000448059.1:p.Ala49Ser
ENST00000307000.7:c.130G>T ENSP00000303500.2:p.Ala44Ser
ENST00000546844.1:c.145G>T ENSP00000446658.1:p.Ala49Ser
ENST00000548677.2:n.232G>T
ENST00000548928.1:n.67G>T
ENST00000549111.5:n.241G>T
ENST00000550978.6:c.129G>T
ENST00000551337.5:c.145G>T ENSP00000447620.1:p.Ala49Ser
ENST00000551988.5:n.234G>T
ENST00000553106.5:c.145G>T ENSP00000448059.1:p.Ala49Ser
ENST00000635500.1:n.113G>T
NM_000277.1:c.145G>T NP_000268.1:p.Ala49Ser
XM_011538422.1:c.145G>T XP_011536724.1:p.Ala49Ser
NM_000277.2:c.145G>T NP_000268.1:p.Ala49Ser
NM_001354304.1:c.145G>T NP_001341233.1:p.Ala49Ser
XM_017019370.2:c.145G>T XP_016874859.1:p.Ala49Ser
NM_000277.3:c.145G>T MANE Select NP_000268.1:p.Ala49Ser
NM_001354304.2:c.145G>T NP_001341233.1:p.Ala49Ser
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