Canonical Allele Identifier: CA377683223

Gene: CYP2C8

Linked Data

• COSMIC: COSM921756 ; COSM4874413 ; COSM4874414
• MyVariant Identifiers: chr10:g.96827092C>G (hg19) ; chr10:g.95067335C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067335C>G , CM000672.2:g.95067335C>G	GRCh38
NC_000010.10:g.96827092C>G , CM000672.1:g.96827092C>G	GRCh37
NC_000010.9:g.96817082C>G	NCBI36
NG_007972.1:g.7163G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.354G>C MANE Select	ENSP00000360317.3:p.Lys118Asn
ENST00000371270.5:c.354G>C	ENSP00000360317.3:p.Lys118Asn
ENST00000479946.2:n.658G>C
ENST00000490994.6:c.*140G>C	ENSP00000433314.1:n.*140G>C
ENST00000525991.5:c.229G>C	ENSP00000433842.1:p.Glu77Gln
ENST00000526814.5:n.609G>C
ENST00000527420.5:c.354G>C	ENSP00000433191.1:p.Lys118Asn
ENST00000527953.5:n.609G>C
ENST00000533320.5:n.588G>C
ENST00000535898.5:c.48G>C	ENSP00000445062.1:p.Lys16Asn
ENST00000539050.5:c.144G>C	ENSP00000442343.2:p.Lys48Asn
ENST00000623108.3:c.144G>C	ENSP00000485110.1:p.Lys48Asn
ENST00000628935.1:c.96G>C	ENSP00000487145.1:p.Lys32Asn
NM_000770.3:c.354G>C MANE Select	NP_000761.3:p.Lys118Asn
NM_001198853.1:c.144G>C	NP_001185782.1:p.Lys48Asn
NM_001198854.1:c.48G>C	NP_001185783.1:p.Lys16Asn
NM_001198855.1:c.144G>C	NP_001185784.1:p.Lys48Asn
XR_945610.1:n.450G>C