Canonical Allele Identifier: CA386493221

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103237478A>C (hg19) ; chr12:g.102843700A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102843700A>C , CM000674.2:g.102843700A>C	GRCh38
NC_000012.11:g.103237478A>C , CM000674.1:g.103237478A>C	GRCh37
NC_000012.10:g.101761608A>C	NCBI36
NG_008690.1:g.78903T>G
NG_008690.2:g.119711T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.1145T>G MANE Select	ENSP00000448059.1:p.Phe382Cys
ENST00000307000.7:c.1130T>G	ENSP00000303500.2:p.Phe377Cys
ENST00000549247.6:n.904T>G
ENST00000551114.2:n.807T>G
ENST00000553106.5:c.1145T>G	ENSP00000448059.1:p.Phe382Cys
ENST00000635477.1:c.249T>G
ENST00000635528.1:n.660T>G
NM_000277.1:c.1145T>G	NP_000268.1:p.Phe382Cys
XM_011538422.1:c.1088T>G	XP_011536724.1:p.Phe363Cys
NM_000277.2:c.1145T>G	NP_000268.1:p.Phe382Cys
NM_001354304.1:c.1145T>G	NP_001341233.1:p.Phe382Cys
NM_000277.3:c.1145T>G MANE Select	NP_000268.1:p.Phe382Cys
NM_001354304.2:c.1145T>G	NP_001341233.1:p.Phe382Cys