Canonical Allele Identifier: CA951231950

Gene: PAH

Linked Data

• dbSNP Id: rs1874858511

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102846690A>C , CM000674.2:g.102846690A>C	GRCh38
NC_000012.11:g.103240468A>C , CM000674.1:g.103240468A>C	GRCh37
NC_000012.10:g.101764598A>C	NCBI36
NG_008690.1:g.75913T>G
NG_008690.2:g.116721T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.969+205T>G MANE Select	ENSP00000448059.1:n.969+205T>G
ENST00000307000.7:c.954+205T>G	ENSP00000303500.2:n.954+205T>G
ENST00000549247.6:n.728+205T>G
ENST00000551114.2:n.631+205T>G
ENST00000553106.5:c.969+205T>G	ENSP00000448059.1:n.969+205T>G
ENST00000635477.1:c.74-2259T>G
ENST00000635528.1:n.484+205T>G
NM_000277.1:c.969+205T>G	NP_000268.1:n.969+205T>G
XM_011538422.1:c.913-2259T>G	XP_011536724.1:n.913-2259T>G
NM_000277.2:c.969+205T>G	NP_000268.1:n.969+205T>G
NM_001354304.1:c.969+205T>G	NP_001341233.1:n.969+205T>G
NM_000277.3:c.969+205T>G MANE Select	NP_000268.1:n.969+205T>G
NM_001354304.2:c.969+205T>G	NP_001341233.1:n.969+205T>G