Canonical Allele Identifier: CA377677344

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796943A>T (hg19) ; chr10:g.95037186A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037186A>T , CM000672.2:g.95037186A>T	GRCh38
NC_000010.10:g.96796943A>T , CM000672.1:g.96796943A>T	GRCh37
NC_000010.9:g.96786933A>T	NCBI36
NG_007972.1:g.37312T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1415T>A MANE Select	ENSP00000360317.3:p.Val472Asp
ENST00000371270.5:c.1415T>A	ENSP00000360317.3:p.Val472Asp
ENST00000490994.6:c.*1201T>A	ENSP00000433314.1:n.*1201T>A
ENST00000525991.5:c.*990T>A	ENSP00000433842.1:n.*990T>A
ENST00000526814.5:n.1670T>A
ENST00000527420.5:c.*272T>A	ENSP00000433191.1:n.*272T>A
ENST00000527953.5:n.1709T>A
ENST00000531714.1:n.603T>A
ENST00000533320.5:n.1649T>A
ENST00000535898.5:c.1109T>A	ENSP00000445062.1:p.Val370Asp
ENST00000539050.5:c.1205T>A	ENSP00000442343.2:p.Val402Asp
ENST00000623108.3:c.1205T>A	ENSP00000485110.1:p.Val402Asp
NM_000770.3:c.1415T>A MANE Select	NP_000761.3:p.Val472Asp
NM_001198853.1:c.1205T>A	NP_001185782.1:p.Val402Asp
NM_001198854.1:c.1109T>A	NP_001185783.1:p.Val370Asp
NM_001198855.1:c.1205T>A	NP_001185784.1:p.Val402Asp
XR_945610.1:n.1550T>A