Canonical Allele Identifier: CA2610269917

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037196-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037197del , CM000672.2:g.95037197del	GRCh38
NC_000010.10:g.96796954del , CM000672.1:g.96796954del	GRCh37
NC_000010.9:g.96786944del	NCBI36
NG_007972.1:g.37301del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1404del MANE Select	ENSP00000360317.3:p.Asn468LysfsTer27
ENST00000371270.5:c.1404del	ENSP00000360317.3:p.Asn468LysfsTer27
ENST00000490994.6:c.*1190del	ENSP00000433314.1:n.*1190del
ENST00000525991.5:c.*979del	ENSP00000433842.1:n.*979del
ENST00000526814.5:n.1659del
ENST00000527420.5:c.*261del	ENSP00000433191.1:n.*261del
ENST00000527953.5:n.1698del
ENST00000531714.1:n.592del
ENST00000533320.5:n.1638del
ENST00000535898.5:c.1098del	ENSP00000445062.1:p.Asn366LysfsTer27
ENST00000539050.5:c.1194del	ENSP00000442343.2:p.Asn398LysfsTer27
ENST00000623108.3:c.1194del	ENSP00000485110.1:p.Asn398LysfsTer27
NM_000770.3:c.1404del MANE Select	NP_000761.3:p.Asn468LysfsTer27
NM_001198853.1:c.1194del	NP_001185782.1:p.Asn398LysfsTer27
NM_001198854.1:c.1098del	NP_001185783.1:p.Asn366LysfsTer27
NM_001198855.1:c.1194del	NP_001185784.1:p.Asn398LysfsTer27
XR_945610.1:n.1539del