Canonical Allele Identifier: CA386296657

Gene: PAH

Linked Data

• ClinVar Variation Id: 1725947
• ClinVar RCV Id: RCV002306918
• MyVariant Identifiers: chr12:g.103248980C>A (hg19) ; chr12:g.102855202C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.102855202C>A , CM000674.2:g.102855202C>A	GRCh38
NC_000012.11:g.103248980C>A , CM000674.1:g.103248980C>A	GRCh37
NC_000012.10:g.101773110C>A	NCBI36
NG_008690.1:g.67401G>T
NG_008690.2:g.108209G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553106.6:c.640G>T MANE Select	ENSP00000448059.1:p.Glu214Ter
ENST00000307000.7:c.625G>T	ENSP00000303500.2:p.Glu209Ter
ENST00000549111.5:n.736G>T
ENST00000553106.5:c.640G>T	ENSP00000448059.1:p.Glu214Ter
NM_000277.1:c.640G>T	NP_000268.1:p.Glu214Ter
XM_011538422.1:c.640G>T	XP_011536724.1:p.Glu214Ter
NM_000277.2:c.640G>T	NP_000268.1:p.Glu214Ter
NM_001354304.1:c.640G>T	NP_001341233.1:p.Glu214Ter
XM_017019370.2:c.640G>T	XP_016874859.1:p.Glu214Ter
NM_000277.3:c.640G>T MANE Select	NP_000268.1:p.Glu214Ter
NM_001354304.2:c.640G>T	NP_001341233.1:p.Glu214Ter