Canonical Allele Identifier: CA386302810
Gene: PAH HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.103306672G>A (hg19) chr12:g.102912894G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102912894G>A , CM000674.2:g.102912894G>A GRCh38
NC_000012.11:g.103306672G>A , CM000674.1:g.103306672G>A GRCh37
NC_000012.10:g.101830802G>A NCBI36
NG_008690.1:g.9709C>T
NG_008690.2:g.50517C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.65C>T MANE Select ENSP00000448059.1:p.Thr22Ile
ENST00000307000.7:c.50C>T ENSP00000303500.2:p.Thr17Ile
ENST00000546844.1:c.65C>T ENSP00000446658.1:p.Thr22Ile
ENST00000548677.2:n.152C>T
ENST00000549111.5:n.161C>T
ENST00000550978.6:c.49C>T
ENST00000551337.5:c.65C>T ENSP00000447620.1:p.Thr22Ile
ENST00000551988.5:n.154C>T
ENST00000553106.5:c.65C>T ENSP00000448059.1:p.Thr22Ile
ENST00000635500.1:n.33C>T
NM_000277.1:c.65C>T NP_000268.1:p.Thr22Ile
XM_011538422.1:c.65C>T XP_011536724.1:p.Thr22Ile
NM_000277.2:c.65C>T NP_000268.1:p.Thr22Ile
NM_001354304.1:c.65C>T NP_001341233.1:p.Thr22Ile
XM_017019370.2:c.65C>T XP_016874859.1:p.Thr22Ile
NM_000277.3:c.65C>T MANE Select NP_000268.1:p.Thr22Ile
NM_001354304.2:c.65C>T NP_001341233.1:p.Thr22Ile
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