Canonical Allele Identifier: CA1929357540

Gene: CYP2C8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95038791C= , CM000672.2:g.95038791C=	GRCh38
NC_000010.10:g.96798548C= , CM000672.1:g.96798548C=	GRCh37
NC_000010.9:g.96788538C=	NCBI36
NG_007972.1:g.35707G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000770.3:c.1291+106G= MANE Select	NP_000761.3:n.1291+106G=
ENST00000371270.6:c.1291+106G= MANE Select	ENSP00000360317.3:n.1291+106G=
NM_001198853.1:c.1081+106G=	NP_001185782.1:n.1081+106G=
NM_001198854.1:c.985+106G=	NP_001185783.1:n.985+106G=
NM_001198855.1:c.1081+106G=	NP_001185784.1:n.1081+106G=
ENST00000371270.5:c.1291+106G=	ENSP00000360317.3:n.1291+106G=
ENST00000490994.6:c.*1077+106G=	ENSP00000433314.1:n.*1077+106G=
ENST00000525991.5:c.*866+106G=	ENSP00000433842.1:n.*866+106G=
ENST00000526814.5:n.1546+106G=
ENST00000527420.5:c.*148+106G=	ENSP00000433191.1:n.*148+106G=
ENST00000527953.5:n.1585+106G=
ENST00000531714.1:n.479+106G=
ENST00000533320.5:n.1525+106G=
ENST00000535898.5:c.985+106G=	ENSP00000445062.1:n.985+106G=
ENST00000539050.5:c.1081+106G=	ENSP00000442343.2:n.1081+106G=
ENST00000623108.3:c.1081+106G=	ENSP00000485110.1:n.1081+106G=
XR_945610.1:n.1426+106G=