Canonical Allele Identifier: CA470841205

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037230-G-A
• MyVariant Identifiers: chr10:g.96796987G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037230G>A , CM000672.2:g.95037230G>A	GRCh38
NC_000010.10:g.96796987G>A , CM000672.1:g.96796987G>A	GRCh37
NC_000010.9:g.96786977G>A	NCBI36
NG_007972.1:g.37268C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1371C>T MANE Select	ENSP00000360317.3:p.Asn457=
ENST00000371270.5:c.1371C>T	ENSP00000360317.3:p.Asn457=
ENST00000490994.6:c.*1157C>T	ENSP00000433314.1:n.*1157C>T
ENST00000525991.5:c.*946C>T	ENSP00000433842.1:n.*946C>T
ENST00000526814.5:n.1626C>T
ENST00000527420.5:c.*228C>T	ENSP00000433191.1:n.*228C>T
ENST00000527953.5:n.1665C>T
ENST00000531714.1:n.559C>T
ENST00000533320.5:n.1605C>T
ENST00000535898.5:c.1065C>T	ENSP00000445062.1:p.Asn355=
ENST00000539050.5:c.1161C>T	ENSP00000442343.2:p.Asn387=
ENST00000623108.3:c.1161C>T	ENSP00000485110.1:p.Asn387=
NM_000770.3:c.1371C>T MANE Select	NP_000761.3:p.Asn457=
NM_001198853.1:c.1161C>T	NP_001185782.1:p.Asn387=
NM_001198854.1:c.1065C>T	NP_001185783.1:p.Asn355=
NM_001198855.1:c.1161C>T	NP_001185784.1:p.Asn387=
XR_945610.1:n.1506C>T