Canonical Allele Identifier: CA377682659

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96826979A>C (hg19) ; chr10:g.95067222A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067222A>C , CM000672.2:g.95067222A>C	GRCh38
NC_000010.10:g.96826979A>C , CM000672.1:g.96826979A>C	GRCh37
NC_000010.9:g.96816969A>C	NCBI36
NG_007972.1:g.7276T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.467T>G MANE Select	ENSP00000360317.3:p.Leu156Trp
ENST00000371270.5:c.467T>G	ENSP00000360317.3:p.Leu156Trp
ENST00000479946.2:n.771T>G
ENST00000490994.6:c.*253T>G	ENSP00000433314.1:n.*253T>G
ENST00000525991.5:c.*42T>G	ENSP00000433842.1:n.*42T>G
ENST00000526814.5:n.722T>G
ENST00000527420.5:c.467T>G	ENSP00000433191.1:p.Leu156Trp
ENST00000527953.5:n.722T>G
ENST00000533320.5:n.701T>G
ENST00000535898.5:c.161T>G	ENSP00000445062.1:p.Leu54Trp
ENST00000539050.5:c.257T>G	ENSP00000442343.2:p.Leu86Trp
ENST00000623108.3:c.257T>G	ENSP00000485110.1:p.Leu86Trp
ENST00000628935.1:c.209T>G	ENSP00000487145.1:p.Leu70Trp
NM_000770.3:c.467T>G MANE Select	NP_000761.3:p.Leu156Trp
NM_001198853.1:c.257T>G	NP_001185782.1:p.Leu86Trp
NM_001198854.1:c.161T>G	NP_001185783.1:p.Leu54Trp
NM_001198855.1:c.257T>G	NP_001185784.1:p.Leu86Trp
XR_945610.1:n.563T>G