Canonical Allele Identifier: CA377677416

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96796976A>G (hg19) ; chr10:g.95037219A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037219A>G , CM000672.2:g.95037219A>G	GRCh38
NC_000010.10:g.96796976A>G , CM000672.1:g.96796976A>G	GRCh37
NC_000010.9:g.96786966A>G	NCBI36
NG_007972.1:g.37279T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1382T>C MANE Select	ENSP00000360317.3:p.Val461Ala
ENST00000371270.5:c.1382T>C	ENSP00000360317.3:p.Val461Ala
ENST00000490994.6:c.*1168T>C	ENSP00000433314.1:n.*1168T>C
ENST00000525991.5:c.*957T>C	ENSP00000433842.1:n.*957T>C
ENST00000526814.5:n.1637T>C
ENST00000527420.5:c.*239T>C	ENSP00000433191.1:n.*239T>C
ENST00000527953.5:n.1676T>C
ENST00000531714.1:n.570T>C
ENST00000533320.5:n.1616T>C
ENST00000535898.5:c.1076T>C	ENSP00000445062.1:p.Val359Ala
ENST00000539050.5:c.1172T>C	ENSP00000442343.2:p.Val391Ala
ENST00000623108.3:c.1172T>C	ENSP00000485110.1:p.Val391Ala
NM_000770.3:c.1382T>C MANE Select	NP_000761.3:p.Val461Ala
NM_001198853.1:c.1172T>C	NP_001185782.1:p.Val391Ala
NM_001198854.1:c.1076T>C	NP_001185783.1:p.Val359Ala
NM_001198855.1:c.1172T>C	NP_001185784.1:p.Val391Ala
XR_945610.1:n.1517T>C