Canonical Allele Identifier: CA377677559

Gene: CYP2C8

Linked Data

• ClinVar Variation Id: 3079524
• ClinVar RCV Id: RCV004367918
• gnomAD v4: 10-95037285-C-T
• MyVariant Identifiers: chr10:g.96797042C>T (hg19) ; chr10:g.95037285C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037285C>T , CM000672.2:g.95037285C>T	GRCh38
NC_000010.10:g.96797042C>T , CM000672.1:g.96797042C>T	GRCh37
NC_000010.9:g.96787032C>T	NCBI36
NG_007972.1:g.37213G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1316G>A MANE Select	ENSP00000360317.3:p.Gly439Glu
ENST00000371270.5:c.1316G>A	ENSP00000360317.3:p.Gly439Glu
ENST00000490994.6:c.*1102G>A	ENSP00000433314.1:n.*1102G>A
ENST00000525991.5:c.*891G>A	ENSP00000433842.1:n.*891G>A
ENST00000526814.5:n.1571G>A
ENST00000527420.5:c.*173G>A	ENSP00000433191.1:n.*173G>A
ENST00000527953.5:n.1610G>A
ENST00000531714.1:n.504G>A
ENST00000533320.5:n.1550G>A
ENST00000535898.5:c.1010G>A	ENSP00000445062.1:p.Gly337Glu
ENST00000539050.5:c.1106G>A	ENSP00000442343.2:p.Gly369Glu
ENST00000623108.3:c.1106G>A	ENSP00000485110.1:p.Gly369Glu
NM_000770.3:c.1316G>A MANE Select	NP_000761.3:p.Gly439Glu
NM_001198853.1:c.1106G>A	NP_001185782.1:p.Gly369Glu
NM_001198854.1:c.1010G>A	NP_001185783.1:p.Gly337Glu
NM_001198855.1:c.1106G>A	NP_001185784.1:p.Gly369Glu
XR_945610.1:n.1451G>A