Canonical Allele Identifier: CA229411
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102575
ClinVar RCV Id: RCV000088811 RCV001380994
dbSNP Id: rs62644467
MyVariant Identifiers: chr12:g.103234256G>T (hg19) chr12:g.102840478G>T (hg38)
ERepo: CA229411/MONDO:0009861/006
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102840478G>T , CM000674.2:g.102840478G>T GRCh38
NC_000012.11:g.103234256G>T , CM000674.1:g.103234256G>T GRCh37
NC_000012.10:g.101758386G>T NCBI36
NG_008690.1:g.82125C>A
NG_008690.2:g.122933C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553106.6:c.1237C>A MANE Select ENSP00000448059.1:p.Arg413Ser
ENST00000307000.7:c.1222C>A ENSP00000303500.2:p.Arg408Ser
ENST00000551114.2:n.899C>A
ENST00000553106.5:c.1237C>A ENSP00000448059.1:p.Arg413Ser
ENST00000635477.1:c.341C>A
ENST00000635528.1:n.752C>A
NM_000277.1:c.1237C>A NP_000268.1:p.Arg413Ser
XM_011538422.1:c.1180C>A XP_011536724.1:p.Arg394Ser
NM_000277.2:c.1237C>A NP_000268.1:p.Arg413Ser
NM_001354304.1:c.1237C>A NP_001341233.1:p.Arg413Ser
NM_000277.3:c.1237C>A MANE Select NP_000268.1:p.Arg413Ser
NM_001354304.2:c.1237C>A NP_001341233.1:p.Arg413Ser
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