Canonical Allele Identifier: CA377683182

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827084T>C (hg19) ; chr10:g.95067327T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067327T>C , CM000672.2:g.95067327T>C	GRCh38
NC_000010.10:g.96827084T>C , CM000672.1:g.96827084T>C	GRCh37
NC_000010.9:g.96817074T>C	NCBI36
NG_007972.1:g.7171A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.362A>G MANE Select	ENSP00000360317.3:p.Lys121Arg
ENST00000371270.5:c.362A>G	ENSP00000360317.3:p.Lys121Arg
ENST00000479946.2:n.666A>G
ENST00000490994.6:c.*148A>G	ENSP00000433314.1:n.*148A>G
ENST00000525991.5:c.237A>G	ENSP00000433842.1:p.Glu79=
ENST00000526814.5:n.617A>G
ENST00000527420.5:c.362A>G	ENSP00000433191.1:p.Lys121Arg
ENST00000527953.5:n.617A>G
ENST00000533320.5:n.596A>G
ENST00000535898.5:c.56A>G	ENSP00000445062.1:p.Lys19Arg
ENST00000539050.5:c.152A>G	ENSP00000442343.2:p.Lys51Arg
ENST00000623108.3:c.152A>G	ENSP00000485110.1:p.Lys51Arg
ENST00000628935.1:c.104A>G	ENSP00000487145.1:p.Lys35Arg
NM_000770.3:c.362A>G MANE Select	NP_000761.3:p.Lys121Arg
NM_001198853.1:c.152A>G	NP_001185782.1:p.Lys51Arg
NM_001198854.1:c.56A>G	NP_001185783.1:p.Lys19Arg
NM_001198855.1:c.152A>G	NP_001185784.1:p.Lys51Arg
XR_945610.1:n.458A>G