Canonical Allele Identifier: CA377677384

Gene: CYP2C8

Linked Data

• COSMIC: COSM4016879 ; COSM4016880
• MyVariant Identifiers: chr10:g.96796963C>A (hg19) ; chr10:g.95037206C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037206C>A , CM000672.2:g.95037206C>A	GRCh38
NC_000010.10:g.96796963C>A , CM000672.1:g.96796963C>A	GRCh37
NC_000010.9:g.96786953C>A	NCBI36
NG_007972.1:g.37292G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1395G>T MANE Select	ENSP00000360317.3:p.Lys465Asn
ENST00000371270.5:c.1395G>T	ENSP00000360317.3:p.Lys465Asn
ENST00000490994.6:c.*1181G>T	ENSP00000433314.1:n.*1181G>T
ENST00000525991.5:c.*970G>T	ENSP00000433842.1:n.*970G>T
ENST00000526814.5:n.1650G>T
ENST00000527420.5:c.*252G>T	ENSP00000433191.1:n.*252G>T
ENST00000527953.5:n.1689G>T
ENST00000531714.1:n.583G>T
ENST00000533320.5:n.1629G>T
ENST00000535898.5:c.1089G>T	ENSP00000445062.1:p.Lys363Asn
ENST00000539050.5:c.1185G>T	ENSP00000442343.2:p.Lys395Asn
ENST00000623108.3:c.1185G>T	ENSP00000485110.1:p.Lys395Asn
NM_000770.3:c.1395G>T MANE Select	NP_000761.3:p.Lys465Asn
NM_001198853.1:c.1185G>T	NP_001185782.1:p.Lys395Asn
NM_001198854.1:c.1089G>T	NP_001185783.1:p.Lys363Asn
NM_001198855.1:c.1185G>T	NP_001185784.1:p.Lys395Asn
XR_945610.1:n.1530G>T