Canonical Allele Identifier: CA377677409

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796973T>A (hg19) ; chr10:g.95037216T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037216T>A , CM000672.2:g.95037216T>A	GRCh38
NC_000010.10:g.96796973T>A , CM000672.1:g.96796973T>A	GRCh37
NC_000010.9:g.96786963T>A	NCBI36
NG_007972.1:g.37282A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1385A>T MANE Select	ENSP00000360317.3:p.Asp462Val
ENST00000371270.5:c.1385A>T	ENSP00000360317.3:p.Asp462Val
ENST00000490994.6:c.*1171A>T	ENSP00000433314.1:n.*1171A>T
ENST00000525991.5:c.*960A>T	ENSP00000433842.1:n.*960A>T
ENST00000526814.5:n.1640A>T
ENST00000527420.5:c.*242A>T	ENSP00000433191.1:n.*242A>T
ENST00000527953.5:n.1679A>T
ENST00000531714.1:n.573A>T
ENST00000533320.5:n.1619A>T
ENST00000535898.5:c.1079A>T	ENSP00000445062.1:p.Asp360Val
ENST00000539050.5:c.1175A>T	ENSP00000442343.2:p.Asp392Val
ENST00000623108.3:c.1175A>T	ENSP00000485110.1:p.Asp392Val
NM_000770.3:c.1385A>T MANE Select	NP_000761.3:p.Asp462Val
NM_001198853.1:c.1175A>T	NP_001185782.1:p.Asp392Val
NM_001198854.1:c.1079A>T	NP_001185783.1:p.Asp360Val
NM_001198855.1:c.1175A>T	NP_001185784.1:p.Asp392Val
XR_945610.1:n.1520A>T