Canonical Allele Identifier: CA386493047

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103234247G>A (hg19) ; chr12:g.102840469G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102840469G>A , CM000674.2:g.102840469G>A	GRCh38
NC_000012.11:g.103234247G>A , CM000674.1:g.103234247G>A	GRCh37
NC_000012.10:g.101758377G>A	NCBI36
NG_008690.1:g.82134C>T
NG_008690.2:g.122942C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.1246C>T MANE Select	ENSP00000448059.1:p.Pro416Ser
ENST00000307000.7:c.1231C>T	ENSP00000303500.2:p.Pro411Ser
ENST00000551114.2:n.908C>T
ENST00000553106.5:c.1246C>T	ENSP00000448059.1:p.Pro416Ser
ENST00000635477.1:c.350C>T
ENST00000635528.1:n.761C>T
NM_000277.1:c.1246C>T	NP_000268.1:p.Pro416Ser
XM_011538422.1:c.1189C>T	XP_011536724.1:p.Pro397Ser
NM_000277.2:c.1246C>T	NP_000268.1:p.Pro416Ser
NM_001354304.1:c.1246C>T	NP_001341233.1:p.Pro416Ser
NM_000277.3:c.1246C>T MANE Select	NP_000268.1:p.Pro416Ser
NM_001354304.2:c.1246C>T	NP_001341233.1:p.Pro416Ser