Canonical Allele Identifier: CA377682601

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95067213-G-T
• COSMIC: COSM4675941 ; COSM4675942 ; COSM4675943
• MyVariant Identifiers: chr10:g.96826970G>T (hg19) ; chr10:g.95067213G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067213G>T , CM000672.2:g.95067213G>T	GRCh38
NC_000010.10:g.96826970G>T , CM000672.1:g.96826970G>T	GRCh37
NC_000010.9:g.96816960G>T	NCBI36
NG_007972.1:g.7285C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.476C>A MANE Select	ENSP00000360317.3:p.Thr159Asn
ENST00000371270.5:c.476C>A	ENSP00000360317.3:p.Thr159Asn
ENST00000479946.2:n.780C>A
ENST00000490994.6:c.*262C>A	ENSP00000433314.1:n.*262C>A
ENST00000525991.5:c.*51C>A	ENSP00000433842.1:n.*51C>A
ENST00000526814.5:n.731C>A
ENST00000527420.5:c.476C>A	ENSP00000433191.1:p.Thr159Asn
ENST00000527953.5:n.731C>A
ENST00000533320.5:n.710C>A
ENST00000535898.5:c.170C>A	ENSP00000445062.1:p.Thr57Asn
ENST00000539050.5:c.266C>A	ENSP00000442343.2:p.Thr89Asn
ENST00000623108.3:c.266C>A	ENSP00000485110.1:p.Thr89Asn
ENST00000628935.1:c.218C>A	ENSP00000487145.1:p.Thr73Asn
NM_000770.3:c.476C>A MANE Select	NP_000761.3:p.Thr159Asn
NM_001198853.1:c.266C>A	NP_001185782.1:p.Thr89Asn
NM_001198854.1:c.170C>A	NP_001185783.1:p.Thr57Asn
NM_001198855.1:c.266C>A	NP_001185784.1:p.Thr89Asn
XR_945610.1:n.572C>A