Canonical Allele Identifier: CA377677528

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037269-C-A
• MyVariant Identifiers: chr10:g.96797026C>A (hg19) ; chr10:g.95037269C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037269C>A , CM000672.2:g.95037269C>A	GRCh38
NC_000010.10:g.96797026C>A , CM000672.1:g.96797026C>A	GRCh37
NC_000010.9:g.96787016C>A	NCBI36
NG_007972.1:g.37229G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1332G>T MANE Select	ENSP00000360317.3:p.Glu444Asp
ENST00000371270.5:c.1332G>T	ENSP00000360317.3:p.Glu444Asp
ENST00000490994.6:c.*1118G>T	ENSP00000433314.1:n.*1118G>T
ENST00000525991.5:c.*907G>T	ENSP00000433842.1:n.*907G>T
ENST00000526814.5:n.1587G>T
ENST00000527420.5:c.*189G>T	ENSP00000433191.1:n.*189G>T
ENST00000527953.5:n.1626G>T
ENST00000531714.1:n.520G>T
ENST00000533320.5:n.1566G>T
ENST00000535898.5:c.1026G>T	ENSP00000445062.1:p.Glu342Asp
ENST00000539050.5:c.1122G>T	ENSP00000442343.2:p.Glu374Asp
ENST00000623108.3:c.1122G>T	ENSP00000485110.1:p.Glu374Asp
NM_000770.3:c.1332G>T MANE Select	NP_000761.3:p.Glu444Asp
NM_001198853.1:c.1122G>T	NP_001185782.1:p.Glu374Asp
NM_001198854.1:c.1026G>T	NP_001185783.1:p.Glu342Asp
NM_001198855.1:c.1122G>T	NP_001185784.1:p.Glu374Asp
XR_945610.1:n.1467G>T