Canonical Allele Identifier: CA670224339

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1205394435
• MyVariant Identifiers: chr10:g.96796853_96796855del (hg19) ; chr10:g.95037096_95037098del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037098_95037100del , CM000672.2:g.95037098_95037100del	GRCh38
NC_000010.10:g.96796855_96796857del , CM000672.1:g.96796855_96796857del	GRCh37
NC_000010.9:g.96786845_96786847del	NCBI36
NG_007972.1:g.37400_37402del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.*30_*32del MANE Select	ENSP00000360317.3:n.*30_*32del
ENST00000371270.5:c.*30_*32del	ENSP00000360317.3:n.*30_*32del
ENST00000490994.6:c.*1289_*1291del	ENSP00000433314.1:n.*1289_*1291del
ENST00000525991.5:c.*1078_*1080del	ENSP00000433842.1:n.*1078_*1080del
ENST00000526814.5:n.1758_1760del
ENST00000527420.5:c.*360_*362del	ENSP00000433191.1:n.*360_*362del
ENST00000527953.5:n.1797_1799del
ENST00000533320.5:n.1737_1739del
ENST00000535898.5:c.*30_*32del	ENSP00000445062.1:n.*30_*32del
ENST00000539050.5:c.*30_*32del	ENSP00000442343.2:n.*30_*32del
ENST00000623108.3:c.*30_*32del	ENSP00000485110.1:n.*30_*32del
NM_000770.3:c.*30_*32del MANE Select	NP_000761.3:n.*30_*32del
NM_001198853.1:c.*30_*32del	NP_001185782.1:n.*30_*32del
NM_001198854.1:c.*30_*32del	NP_001185783.1:n.*30_*32del
NM_001198855.1:c.*30_*32del	NP_001185784.1:n.*30_*32del