Canonical Allele Identifier: CA481331529

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103246679C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102852901C>G , CM000674.2:g.102852901C>G	GRCh38
NC_000012.11:g.103246679C>G , CM000674.1:g.103246679C>G	GRCh37
NC_000012.10:g.101770809C>G	NCBI36
NG_008690.1:g.69702G>C
NG_008690.2:g.110510G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.756G>C MANE Select	ENSP00000448059.1:p.Arg252=
ENST00000307000.7:c.741G>C	ENSP00000303500.2:p.Arg247=
ENST00000549247.6:n.515G>C
ENST00000553106.5:c.756G>C	ENSP00000448059.1:p.Arg252=
NM_000277.1:c.756G>C	NP_000268.1:p.Arg252=
XM_011538422.1:c.756G>C	XP_011536724.1:p.Arg252=
NM_000277.2:c.756G>C	NP_000268.1:p.Arg252=
NM_001354304.1:c.756G>C	NP_001341233.1:p.Arg252=
NM_000277.3:c.756G>C MANE Select	NP_000268.1:p.Arg252=
NM_001354304.2:c.756G>C	NP_001341233.1:p.Arg252=