Canonical Allele Identifier: CA386294559

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103246617G>T (hg19) ; chr12:g.102852839G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102852839G>T , CM000674.2:g.102852839G>T	GRCh38
NC_000012.11:g.103246617G>T , CM000674.1:g.103246617G>T	GRCh37
NC_000012.10:g.101770747G>T	NCBI36
NG_008690.1:g.69764C>A
NG_008690.2:g.110572C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.818C>A MANE Select	ENSP00000448059.1:p.Ser273Tyr
ENST00000307000.7:c.803C>A	ENSP00000303500.2:p.Ser268Tyr
ENST00000549247.6:n.577C>A
ENST00000553106.5:c.818C>A	ENSP00000448059.1:p.Ser273Tyr
NM_000277.1:c.818C>A	NP_000268.1:p.Ser273Tyr
XM_011538422.1:c.818C>A	XP_011536724.1:p.Ser273Tyr
NM_000277.2:c.818C>A	NP_000268.1:p.Ser273Tyr
NM_001354304.1:c.818C>A	NP_001341233.1:p.Ser273Tyr
NM_000277.3:c.818C>A MANE Select	NP_000268.1:p.Ser273Tyr
NM_001354304.2:c.818C>A	NP_001341233.1:p.Ser273Tyr