Canonical Allele Identifier: CA386294569

Gene: PAH

Linked Data

• MyVariant Identifiers: chr12:g.103246624G>C (hg19) ; chr12:g.102852846G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102852846G>C , CM000674.2:g.102852846G>C	GRCh38
NC_000012.11:g.103246624G>C , CM000674.1:g.103246624G>C	GRCh37
NC_000012.10:g.101770754G>C	NCBI36
NG_008690.1:g.69757C>G
NG_008690.2:g.110565C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553106.6:c.811C>G MANE Select	ENSP00000448059.1:p.His271Asp
ENST00000307000.7:c.796C>G	ENSP00000303500.2:p.His266Asp
ENST00000549247.6:n.570C>G
ENST00000553106.5:c.811C>G	ENSP00000448059.1:p.His271Asp
NM_000277.1:c.811C>G	NP_000268.1:p.His271Asp
XM_011538422.1:c.811C>G	XP_011536724.1:p.His271Asp
NM_000277.2:c.811C>G	NP_000268.1:p.His271Asp
NM_001354304.1:c.811C>G	NP_001341233.1:p.His271Asp
NM_000277.3:c.811C>G MANE Select	NP_000268.1:p.His271Asp
NM_001354304.2:c.811C>G	NP_001341233.1:p.His271Asp