Canonical Allele Identifier: CA377677487

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797007T>G (hg19) ; chr10:g.95037250T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037250T>G , CM000672.2:g.95037250T>G	GRCh38
NC_000010.10:g.96797007T>G , CM000672.1:g.96797007T>G	GRCh37
NC_000010.9:g.96786997T>G	NCBI36
NG_007972.1:g.37248A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1351A>C MANE Select	ENSP00000360317.3:p.Thr451Pro
ENST00000371270.5:c.1351A>C	ENSP00000360317.3:p.Thr451Pro
ENST00000490994.6:c.*1137A>C	ENSP00000433314.1:n.*1137A>C
ENST00000525991.5:c.*926A>C	ENSP00000433842.1:n.*926A>C
ENST00000526814.5:n.1606A>C
ENST00000527420.5:c.*208A>C	ENSP00000433191.1:n.*208A>C
ENST00000527953.5:n.1645A>C
ENST00000531714.1:n.539A>C
ENST00000533320.5:n.1585A>C
ENST00000535898.5:c.1045A>C	ENSP00000445062.1:p.Thr349Pro
ENST00000539050.5:c.1141A>C	ENSP00000442343.2:p.Thr381Pro
ENST00000623108.3:c.1141A>C	ENSP00000485110.1:p.Thr381Pro
NM_000770.3:c.1351A>C MANE Select	NP_000761.3:p.Thr451Pro
NM_001198853.1:c.1141A>C	NP_001185782.1:p.Thr381Pro
NM_001198854.1:c.1045A>C	NP_001185783.1:p.Thr349Pro
NM_001198855.1:c.1141A>C	NP_001185784.1:p.Thr381Pro
XR_945610.1:n.1486A>C