Canonical Allele Identifier: CA682822204

Gene: PAH

Linked Data

• dbSNP Id: rs1391511619
• MyVariant Identifiers: chr12:g.103237387C>A (hg19) ; chr12:g.102843609C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102843609C>A , CM000674.2:g.102843609C>A	GRCh38
NC_000012.11:g.103237387C>A , CM000674.1:g.103237387C>A	GRCh37
NC_000012.10:g.101761517C>A	NCBI36
NG_008690.1:g.78994G>T
NG_008690.2:g.119802G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.1199+37G>T MANE Select	ENSP00000448059.1:n.1199+37G>T
ENST00000307000.7:c.1184+37G>T	ENSP00000303500.2:n.1184+37G>T
ENST00000549247.6:n.958+37G>T
ENST00000551114.2:n.861+37G>T
ENST00000553106.5:c.1199+37G>T	ENSP00000448059.1:n.1199+37G>T
ENST00000635477.1:c.303+37G>T
ENST00000635528.1:n.714+37G>T
NM_000277.1:c.1199+37G>T	NP_000268.1:n.1199+37G>T
XM_011538422.1:c.1142+37G>T	XP_011536724.1:n.1142+37G>T
NM_000277.2:c.1199+37G>T	NP_000268.1:n.1199+37G>T
NM_001354304.1:c.1199+37G>T	NP_001341233.1:n.1199+37G>T
NM_000277.3:c.1199+37G>T MANE Select	NP_000268.1:n.1199+37G>T
NM_001354304.2:c.1199+37G>T	NP_001341233.1:n.1199+37G>T