Canonical Allele Identifier: CA1167214995

Gene: CPT2

Linked Data

• dbSNP Id: rs1645410737
• gnomAD v4: 1-53209963-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53209963T>A , CM000663.2:g.53209963T>A	GRCh38
NC_000001.10:g.53675635T>A , CM000663.1:g.53675635T>A	GRCh37
NC_000001.9:g.53448223T>A	NCBI36
NG_008035.1:g.18535T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371486.4:c.341-52T>A MANE Select	ENSP00000360541.3:n.341-52T>A
ENST00000635862.1:c.341-52T>A	ENSP00000490867.1:n.341-52T>A
ENST00000635888.1:c.*327-52T>A	ENSP00000490042.1:n.*327-52T>A
ENST00000636239.1:c.234-52T>A	ENSP00000490066.1:n.234-52T>A
ENST00000636867.1:c.341-52T>A	ENSP00000489631.1:n.341-52T>A
ENST00000636891.1:c.341-52T>A	ENSP00000490399.1:n.341-52T>A
ENST00000636935.1:c.341-3301T>A	ENSP00000489757.1:n.341-3301T>A
ENST00000637252.1:c.341-52T>A	ENSP00000490492.1:n.341-52T>A
ENST00000637726.1:n.2489T>A
ENST00000638135.1:c.153-52T>A	ENSP00000489756.1:n.153-52T>A
ENST00000371486.3:c.341-52T>A	ENSP00000360541.3:n.341-52T>A
NM_000098.2:c.341-52T>A	NP_000089.1:n.341-52T>A
XM_005270484.1:c.341-52T>A	XP_005270541.1:n.341-52T>A
NM_001330589.1:c.341-52T>A	NP_001317518.1:n.341-52T>A
NM_000098.3:c.341-52T>A MANE Select	NP_000089.1:n.341-52T>A
NM_001330589.2:c.341-52T>A	NP_001317518.1:n.341-52T>A