Canonical Allele Identifier: CA386492953
Gene: PAH HGNC NCBI

Linked Data

gnomAD v4: 12-102840420-A-G
MyVariant Identifiers: chr12:g.103234198A>G (hg19) chr12:g.102840420A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840420A>G , CM000674.2:g.102840420A>G GRCh38
NC_000012.11:g.103234198A>G , CM000674.1:g.103234198A>G GRCh37
NC_000012.10:g.101758328A>G NCBI36
NG_008690.1:g.82183T>C
NG_008690.2:g.122991T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000553106.6:c.1295T>C MANE Select ENSP00000448059.1:p.Ile432Thr
ENST00000307000.7:c.1280T>C ENSP00000303500.2:p.Ile427Thr
ENST00000551114.2:n.957T>C
ENST00000553106.5:c.1295T>C ENSP00000448059.1:p.Ile432Thr
ENST00000635477.1:c.399T>C
ENST00000635528.1:n.810T>C
NM_000277.1:c.1295T>C NP_000268.1:p.Ile432Thr
XM_011538422.1:c.1238T>C XP_011536724.1:p.Ile413Thr
NM_000277.2:c.1295T>C NP_000268.1:p.Ile432Thr
NM_001354304.1:c.1295T>C NP_001341233.1:p.Ile432Thr
NM_000277.3:c.1295T>C MANE Select NP_000268.1:p.Ile432Thr
NM_001354304.2:c.1295T>C NP_001341233.1:p.Ile432Thr
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