Canonical Allele Identifier: CA290511

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53202391C>T , CM000663.2:g.53202391C>T	GRCh38
NC_000001.10:g.53668063C>T , CM000663.1:g.53668063C>T	GRCh37
NC_000001.9:g.53440651C>T	NCBI36
NG_008035.1:g.10963C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.302C>T MANE Select	ENSP00000360541.3:p.Ala101Val
ENST00000468572.2:n.387C>T
ENST00000635862.1:c.302C>T	ENSP00000490867.1:p.Ala101Val
ENST00000635888.1:c.*288C>T	ENSP00000490042.1:n.*288C>T
ENST00000636239.1:c.233+1592C>T	ENSP00000490066.1:n.233+1592C>T
ENST00000636673.1:n.2615C>T
ENST00000636867.1:c.302C>T	ENSP00000489631.1:p.Ala101Val
ENST00000636891.1:c.302C>T	ENSP00000490399.1:p.Ala101Val
ENST00000636935.1:c.302C>T	ENSP00000489757.1:p.Ala101Val
ENST00000637252.1:c.302C>T	ENSP00000490492.1:p.Ala101Val
ENST00000638135.1:c.152+5296C>T	ENSP00000489756.1:n.152+5296C>T
ENST00000371486.3:c.302C>T	ENSP00000360541.3:p.Ala101Val
ENST00000468572.1:n.387C>T
NM_000098.2:c.302C>T	NP_000089.1:p.Ala101Val
XM_005270484.1:c.302C>T	XP_005270541.1:p.Ala101Val
NM_001330589.1:c.302C>T	NP_001317518.1:p.Ala101Val
NM_000098.3:c.302C>T MANE Select	NP_000089.1:p.Ala101Val
NM_001330589.2:c.302C>T	NP_001317518.1:p.Ala101Val