Canonical Allele Identifier: CA481375769

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103238162G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102844384G>C , CM000674.2:g.102844384G>C	GRCh38
NC_000012.11:g.103238162G>C , CM000674.1:g.103238162G>C	GRCh37
NC_000012.10:g.101762292G>C	NCBI36
NG_008690.1:g.78219C>G
NG_008690.2:g.119027C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.1017C>G MANE Select	ENSP00000448059.1:p.Ser339=
ENST00000307000.7:c.1002C>G	ENSP00000303500.2:p.Ser334=
ENST00000549247.6:n.776C>G
ENST00000551114.2:n.679C>G
ENST00000553106.5:c.1017C>G	ENSP00000448059.1:p.Ser339=
ENST00000635477.1:c.121C>G
ENST00000635528.1:n.532C>G
NM_000277.1:c.1017C>G	NP_000268.1:p.Ser339=
XM_011538422.1:c.960C>G	XP_011536724.1:p.Ser320=
NM_000277.2:c.1017C>G	NP_000268.1:p.Ser339=
NM_001354304.1:c.1017C>G	NP_001341233.1:p.Ser339=
NM_000277.3:c.1017C>G MANE Select	NP_000268.1:p.Ser339=
NM_001354304.2:c.1017C>G	NP_001341233.1:p.Ser339=