Canonical Allele Identifier: CA481375646

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103237498T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102843720T>C , CM000674.2:g.102843720T>C	GRCh38
NC_000012.11:g.103237498T>C , CM000674.1:g.103237498T>C	GRCh37
NC_000012.10:g.101761628T>C	NCBI36
NG_008690.1:g.78883A>G
NG_008690.2:g.119691A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.1125A>G MANE Select	ENSP00000448059.1:p.Gln375=
ENST00000307000.7:c.1110A>G	ENSP00000303500.2:p.Gln370=
ENST00000549247.6:n.884A>G
ENST00000551114.2:n.787A>G
ENST00000553106.5:c.1125A>G	ENSP00000448059.1:p.Gln375=
ENST00000635477.1:c.229A>G
ENST00000635528.1:n.640A>G
NM_000277.1:c.1125A>G	NP_000268.1:p.Gln375=
XM_011538422.1:c.1068A>G	XP_011536724.1:p.Gln356=
NM_000277.2:c.1125A>G	NP_000268.1:p.Gln375=
NM_001354304.1:c.1125A>G	NP_001341233.1:p.Gln375=
NM_000277.3:c.1125A>G MANE Select	NP_000268.1:p.Gln375=
NM_001354304.2:c.1125A>G	NP_001341233.1:p.Gln375=