Canonical Allele Identifier: CA386295281

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103246633A>C (hg19) ; chr12:g.102852855A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102852855A>C , CM000674.2:g.102852855A>C	GRCh38
NC_000012.11:g.103246633A>C , CM000674.1:g.103246633A>C	GRCh37
NC_000012.10:g.101770763A>C	NCBI36
NG_008690.1:g.69748T>G
NG_008690.2:g.110556T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.802T>G MANE Select	ENSP00000448059.1:p.Tyr268Asp
ENST00000307000.7:c.787T>G	ENSP00000303500.2:p.Tyr263Asp
ENST00000549247.6:n.561T>G
ENST00000553106.5:c.802T>G	ENSP00000448059.1:p.Tyr268Asp
NM_000277.1:c.802T>G	NP_000268.1:p.Tyr268Asp
XM_011538422.1:c.802T>G	XP_011536724.1:p.Tyr268Asp
NM_000277.2:c.802T>G	NP_000268.1:p.Tyr268Asp
NM_001354304.1:c.802T>G	NP_001341233.1:p.Tyr268Asp
NM_000277.3:c.802T>G MANE Select	NP_000268.1:p.Tyr268Asp
NM_001354304.2:c.802T>G	NP_001341233.1:p.Tyr268Asp