Canonical Allele Identifier: CA858950

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53202447T>A , CM000663.2:g.53202447T>A	GRCh38
NC_000001.10:g.53668119T>A , CM000663.1:g.53668119T>A	GRCh37
NC_000001.9:g.53440707T>A	NCBI36
NG_008035.1:g.11019T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000098.3:c.340+18T>A MANE Select	NP_000089.1:n.340+18T>A
ENST00000371486.4:c.340+18T>A MANE Select	ENSP00000360541.3:n.340+18T>A
NM_000098.2:c.340+18T>A	NP_000089.1:n.340+18T>A
NM_001330589.1:c.340+18T>A	NP_001317518.1:n.340+18T>A
NM_001330589.2:c.340+18T>A	NP_001317518.1:n.340+18T>A
ENST00000371486.3:c.340+18T>A	ENSP00000360541.3:n.340+18T>A
ENST00000468572.1:n.443T>A
ENST00000468572.2:n.443T>A
ENST00000635862.1:c.340+18T>A	ENSP00000490867.1:n.340+18T>A
ENST00000635888.1:c.*326+18T>A	ENSP00000490042.1:n.*326+18T>A
ENST00000636239.1:c.233+1648T>A	ENSP00000490066.1:n.233+1648T>A
ENST00000636673.1:n.2671T>A
ENST00000636867.1:c.340+18T>A	ENSP00000489631.1:n.340+18T>A
ENST00000636891.1:c.340+18T>A	ENSP00000490399.1:n.340+18T>A
ENST00000636935.1:c.340+18T>A	ENSP00000489757.1:n.340+18T>A
ENST00000637252.1:c.340+18T>A	ENSP00000490492.1:n.340+18T>A
ENST00000638135.1:c.152+5352T>A	ENSP00000489756.1:n.152+5352T>A
XM_005270484.1:c.340+18T>A	XP_005270541.1:n.340+18T>A