Canonical Allele Identifier: CA377677441

Gene: CYP2C8

Linked Data

• COSMIC: COSM3442024 ; COSM3442025
• MyVariant Identifiers: chr10:g.96796988T>A (hg19) ; chr10:g.95037231T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037231T>A , CM000672.2:g.95037231T>A	GRCh38
NC_000010.10:g.96796988T>A , CM000672.1:g.96796988T>A	GRCh37
NC_000010.9:g.96786978T>A	NCBI36
NG_007972.1:g.37267A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1370A>T MANE Select	ENSP00000360317.3:p.Asn457Ile
ENST00000371270.5:c.1370A>T	ENSP00000360317.3:p.Asn457Ile
ENST00000490994.6:c.*1156A>T	ENSP00000433314.1:n.*1156A>T
ENST00000525991.5:c.*945A>T	ENSP00000433842.1:n.*945A>T
ENST00000526814.5:n.1625A>T
ENST00000527420.5:c.*227A>T	ENSP00000433191.1:n.*227A>T
ENST00000527953.5:n.1664A>T
ENST00000531714.1:n.558A>T
ENST00000533320.5:n.1604A>T
ENST00000535898.5:c.1064A>T	ENSP00000445062.1:p.Asn355Ile
ENST00000539050.5:c.1160A>T	ENSP00000442343.2:p.Asn387Ile
ENST00000623108.3:c.1160A>T	ENSP00000485110.1:p.Asn387Ile
NM_000770.3:c.1370A>T MANE Select	NP_000761.3:p.Asn457Ile
NM_001198853.1:c.1160A>T	NP_001185782.1:p.Asn387Ile
NM_001198854.1:c.1064A>T	NP_001185783.1:p.Asn355Ile
NM_001198855.1:c.1160A>T	NP_001185784.1:p.Asn387Ile
XR_945610.1:n.1505A>T