Canonical Allele Identifier: CA377677245

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796894G>C (hg19) ; chr10:g.95037137G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037137G>C , CM000672.2:g.95037137G>C	GRCh38
NC_000010.10:g.96796894G>C , CM000672.1:g.96796894G>C	GRCh37
NC_000010.9:g.96786884G>C	NCBI36
NG_007972.1:g.37361C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1464C>G MANE Select	ENSP00000360317.3:p.Ile488Met
ENST00000371270.5:c.1464C>G	ENSP00000360317.3:p.Ile488Met
ENST00000490994.6:c.*1250C>G	ENSP00000433314.1:n.*1250C>G
ENST00000525991.5:c.*1039C>G	ENSP00000433842.1:n.*1039C>G
ENST00000526814.5:n.1719C>G
ENST00000527420.5:c.*321C>G	ENSP00000433191.1:n.*321C>G
ENST00000527953.5:n.1758C>G
ENST00000533320.5:n.1698C>G
ENST00000535898.5:c.1158C>G	ENSP00000445062.1:p.Ile386Met
ENST00000539050.5:c.1254C>G	ENSP00000442343.2:p.Ile418Met
ENST00000623108.3:c.1254C>G	ENSP00000485110.1:p.Ile418Met
NM_000770.3:c.1464C>G MANE Select	NP_000761.3:p.Ile488Met
NM_001198853.1:c.1254C>G	NP_001185782.1:p.Ile418Met
NM_001198854.1:c.1158C>G	NP_001185783.1:p.Ile386Met
NM_001198855.1:c.1254C>G	NP_001185784.1:p.Ile418Met