Canonical Allele Identifier: CA2610271386

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95068569-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95068570del , CM000672.2:g.95068570del	GRCh38
NC_000010.10:g.96828327del , CM000672.1:g.96828327del	GRCh37
NC_000010.9:g.96818317del	NCBI36
NG_007972.1:g.5928del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371270.6:c.168+665del MANE Select	ENSP00000360317.3:n.168+665del
ENST00000371270.5:c.168+665del	ENSP00000360317.3:n.168+665del
ENST00000479946.2:n.301+627del
ENST00000490994.6:c.206+627del	ENSP00000433314.1:n.206+627del
ENST00000525991.5:c.206+627del	ENSP00000433842.1:n.206+627del
ENST00000526814.5:n.252+665del
ENST00000527420.5:c.168+665del	ENSP00000433191.1:n.168+665del
ENST00000527953.5:n.252+665del
ENST00000533320.5:n.231+627del
ENST00000535898.5:c.25+627del	ENSP00000445062.1:n.25+627del
ENST00000539050.5:c.-46del	ENSP00000442343.2:n.-46del
ENST00000623108.3:c.-43+627del	ENSP00000485110.1:n.-43+627del
NM_000770.3:c.168+665del MANE Select	NP_000761.3:n.168+665del
NM_001198853.1:c.-43+627del	NP_001185782.1:n.-43+627del
NM_001198854.1:c.25+627del	NP_001185783.1:n.25+627del
NM_001198855.1:c.-46del	NP_001185784.1:n.-46del
XR_945610.1:n.264+665del