Canonical Allele Identifier: CA377682952

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827028T>A (hg19) ; chr10:g.95067271T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067271T>A , CM000672.2:g.95067271T>A	GRCh38
NC_000010.10:g.96827028T>A , CM000672.1:g.96827028T>A	GRCh37
NC_000010.9:g.96817018T>A	NCBI36
NG_007972.1:g.7227A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.418A>T MANE Select	ENSP00000360317.3:p.Ser140Cys
ENST00000371270.5:c.418A>T	ENSP00000360317.3:p.Ser140Cys
ENST00000479946.2:n.722A>T
ENST00000490994.6:c.*204A>T	ENSP00000433314.1:n.*204A>T
ENST00000525991.5:c.293A>T	ENSP00000433842.1:p.Glu98Val
ENST00000526814.5:n.673A>T
ENST00000527420.5:c.418A>T	ENSP00000433191.1:p.Ser140Cys
ENST00000527953.5:n.673A>T
ENST00000533320.5:n.652A>T
ENST00000535898.5:c.112A>T	ENSP00000445062.1:p.Ser38Cys
ENST00000539050.5:c.208A>T	ENSP00000442343.2:p.Ser70Cys
ENST00000623108.3:c.208A>T	ENSP00000485110.1:p.Ser70Cys
ENST00000628935.1:c.160A>T	ENSP00000487145.1:p.Ser54Cys
NM_000770.3:c.418A>T MANE Select	NP_000761.3:p.Ser140Cys
NM_001198853.1:c.208A>T	NP_001185782.1:p.Ser70Cys
NM_001198854.1:c.112A>T	NP_001185783.1:p.Ser38Cys
NM_001198855.1:c.208A>T	NP_001185784.1:p.Ser70Cys
XR_945610.1:n.514A>T