Canonical Allele Identifier: CA377677288

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796913G>T (hg19) ; chr10:g.95037156G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037156G>T , CM000672.2:g.95037156G>T	GRCh38
NC_000010.10:g.96796913G>T , CM000672.1:g.96796913G>T	GRCh37
NC_000010.9:g.96786903G>T	NCBI36
NG_007972.1:g.37342C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1445C>A MANE Select	ENSP00000360317.3:p.Ser482Ter
ENST00000371270.5:c.1445C>A	ENSP00000360317.3:p.Ser482Ter
ENST00000490994.6:c.*1231C>A	ENSP00000433314.1:n.*1231C>A
ENST00000525991.5:c.*1020C>A	ENSP00000433842.1:n.*1020C>A
ENST00000526814.5:n.1700C>A
ENST00000527420.5:c.*302C>A	ENSP00000433191.1:n.*302C>A
ENST00000527953.5:n.1739C>A
ENST00000533320.5:n.1679C>A
ENST00000535898.5:c.1139C>A	ENSP00000445062.1:p.Ser380Ter
ENST00000539050.5:c.1235C>A	ENSP00000442343.2:p.Ser412Ter
ENST00000623108.3:c.1235C>A	ENSP00000485110.1:p.Ser412Ter
NM_000770.3:c.1445C>A MANE Select	NP_000761.3:p.Ser482Ter
NM_001198853.1:c.1235C>A	NP_001185782.1:p.Ser412Ter
NM_001198854.1:c.1139C>A	NP_001185783.1:p.Ser380Ter
NM_001198855.1:c.1235C>A	NP_001185784.1:p.Ser412Ter