Canonical Allele Identifier: CA931389201

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1337091909
• gnomAD v3: 10-95037620-T-TA
• gnomAD v4: 10-95037620-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037624dup , CM000672.2:g.95037624dup	GRCh38
NC_000010.10:g.96797381dup , CM000672.1:g.96797381dup	GRCh37
NC_000010.9:g.96787371dup	NCBI36
NG_007972.1:g.36877dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.1292-312dup MANE Select	ENSP00000360317.3:n.1292-312dup
ENST00000371270.5:c.1292-312dup	ENSP00000360317.3:n.1292-312dup
ENST00000490994.6:c.*1078-312dup	ENSP00000433314.1:n.*1078-312dup
ENST00000525991.5:c.*867-312dup	ENSP00000433842.1:n.*867-312dup
ENST00000526814.5:n.1547-312dup
ENST00000527420.5:c.*149-312dup	ENSP00000433191.1:n.*149-312dup
ENST00000527953.5:n.1586-312dup
ENST00000531714.1:n.480-312dup
ENST00000533320.5:n.1526-312dup
ENST00000535898.5:c.986-312dup	ENSP00000445062.1:n.986-312dup
ENST00000539050.5:c.1082-312dup	ENSP00000442343.2:n.1082-312dup
ENST00000623108.3:c.1082-312dup	ENSP00000485110.1:n.1082-312dup
NM_000770.3:c.1292-312dup MANE Select	NP_000761.3:n.1292-312dup
NM_001198853.1:c.1082-312dup	NP_001185782.1:n.1082-312dup
NM_001198854.1:c.986-312dup	NP_001185783.1:n.986-312dup
NM_001198855.1:c.1082-312dup	NP_001185784.1:n.1082-312dup
XR_945610.1:n.1427-312dup