Canonical Allele Identifier: CA470841209

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797001A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037244A>G , CM000672.2:g.95037244A>G	GRCh38
NC_000010.10:g.96797001A>G , CM000672.1:g.96797001A>G	GRCh37
NC_000010.9:g.96786991A>G	NCBI36
NG_007972.1:g.37254T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1357T>C MANE Select	ENSP00000360317.3:p.Leu453=
ENST00000371270.5:c.1357T>C	ENSP00000360317.3:p.Leu453=
ENST00000490994.6:c.*1143T>C	ENSP00000433314.1:n.*1143T>C
ENST00000525991.5:c.*932T>C	ENSP00000433842.1:n.*932T>C
ENST00000526814.5:n.1612T>C
ENST00000527420.5:c.*214T>C	ENSP00000433191.1:n.*214T>C
ENST00000527953.5:n.1651T>C
ENST00000531714.1:n.545T>C
ENST00000533320.5:n.1591T>C
ENST00000535898.5:c.1051T>C	ENSP00000445062.1:p.Leu351=
ENST00000539050.5:c.1147T>C	ENSP00000442343.2:p.Leu383=
ENST00000623108.3:c.1147T>C	ENSP00000485110.1:p.Leu383=
NM_000770.3:c.1357T>C MANE Select	NP_000761.3:p.Leu453=
NM_001198853.1:c.1147T>C	NP_001185782.1:p.Leu383=
NM_001198854.1:c.1051T>C	NP_001185783.1:p.Leu351=
NM_001198855.1:c.1147T>C	NP_001185784.1:p.Leu383=
XR_945610.1:n.1492T>C