Canonical Allele Identifier: CA377677537

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797030A>C (hg19) ; chr10:g.95037273A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037273A>C , CM000672.2:g.95037273A>C	GRCh38
NC_000010.10:g.96797030A>C , CM000672.1:g.96797030A>C	GRCh37
NC_000010.9:g.96787020A>C	NCBI36
NG_007972.1:g.37225T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1328T>G MANE Select	ENSP00000360317.3:p.Met443Arg
ENST00000371270.5:c.1328T>G	ENSP00000360317.3:p.Met443Arg
ENST00000490994.6:c.*1114T>G	ENSP00000433314.1:n.*1114T>G
ENST00000525991.5:c.*903T>G	ENSP00000433842.1:n.*903T>G
ENST00000526814.5:n.1583T>G
ENST00000527420.5:c.*185T>G	ENSP00000433191.1:n.*185T>G
ENST00000527953.5:n.1622T>G
ENST00000531714.1:n.516T>G
ENST00000533320.5:n.1562T>G
ENST00000535898.5:c.1022T>G	ENSP00000445062.1:p.Met341Arg
ENST00000539050.5:c.1118T>G	ENSP00000442343.2:p.Met373Arg
ENST00000623108.3:c.1118T>G	ENSP00000485110.1:p.Met373Arg
NM_000770.3:c.1328T>G MANE Select	NP_000761.3:p.Met443Arg
NM_001198853.1:c.1118T>G	NP_001185782.1:p.Met373Arg
NM_001198854.1:c.1022T>G	NP_001185783.1:p.Met341Arg
NM_001198855.1:c.1118T>G	NP_001185784.1:p.Met373Arg
XR_945610.1:n.1463T>G