Canonical Allele Identifier: CA377682738

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96826994C>A (hg19) ; chr10:g.95067237C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067237C>A , CM000672.2:g.95067237C>A	GRCh38
NC_000010.10:g.96826994C>A , CM000672.1:g.96826994C>A	GRCh37
NC_000010.9:g.96816984C>A	NCBI36
NG_007972.1:g.7261G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.452G>T MANE Select	ENSP00000360317.3:p.Cys151Phe
ENST00000371270.5:c.452G>T	ENSP00000360317.3:p.Cys151Phe
ENST00000479946.2:n.756G>T
ENST00000490994.6:c.*238G>T	ENSP00000433314.1:n.*238G>T
ENST00000525991.5:c.*27G>T	ENSP00000433842.1:n.*27G>T
ENST00000526814.5:n.707G>T
ENST00000527420.5:c.452G>T	ENSP00000433191.1:p.Cys151Phe
ENST00000527953.5:n.707G>T
ENST00000533320.5:n.686G>T
ENST00000535898.5:c.146G>T	ENSP00000445062.1:p.Cys49Phe
ENST00000539050.5:c.242G>T	ENSP00000442343.2:p.Cys81Phe
ENST00000623108.3:c.242G>T	ENSP00000485110.1:p.Cys81Phe
ENST00000628935.1:c.194G>T	ENSP00000487145.1:p.Cys65Phe
NM_000770.3:c.452G>T MANE Select	NP_000761.3:p.Cys151Phe
NM_001198853.1:c.242G>T	NP_001185782.1:p.Cys81Phe
NM_001198854.1:c.146G>T	NP_001185783.1:p.Cys49Phe
NM_001198855.1:c.242G>T	NP_001185784.1:p.Cys81Phe
XR_945610.1:n.548G>T