Canonical Allele Identifier: CA340395163

Gene: CPT2

Linked Data

• dbSNP Id: rs74315297
• gnomAD v3: 1-53211016-T-G
• gnomAD v4: 1-53211016-T-G
• MyVariant Identifiers: chr1:g.53676688T>G (hg19) ; chr1:g.53211016T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53211016T>G , CM000663.2:g.53211016T>G	GRCh38
NC_000001.10:g.53676688T>G , CM000663.1:g.53676688T>G	GRCh37
NC_000001.9:g.53449276T>G	NCBI36
NG_008035.1:g.19588T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1342T>G MANE Select	ENSP00000360541.3:p.Phe448Val
ENST00000635862.1:c.1342T>G	ENSP00000490867.1:p.Phe448Val
ENST00000635888.1:c.*1328T>G	ENSP00000490042.1:n.*1328T>G
ENST00000636239.1:c.*989T>G	ENSP00000490066.1:n.*989T>G
ENST00000636867.1:c.1342T>G	ENSP00000489631.1:p.Phe448Val
ENST00000636891.1:c.1342T>G	ENSP00000490399.1:p.Phe448Val
ENST00000636935.1:c.341-2248T>G	ENSP00000489757.1:n.341-2248T>G
ENST00000637252.1:c.1342T>G	ENSP00000490492.1:p.Phe448Val
ENST00000637726.1:n.3542T>G
ENST00000638135.1:c.*989T>G	ENSP00000489756.1:n.*989T>G
ENST00000371486.3:c.1342T>G	ENSP00000360541.3:p.Phe448Val
NM_000098.2:c.1342T>G	NP_000089.1:p.Phe448Val
XM_005270484.1:c.1342T>G	XP_005270541.1:p.Phe448Val
NM_001330589.1:c.1342T>G	NP_001317518.1:p.Phe448Val
NM_000098.3:c.1342T>G MANE Select	NP_000089.1:p.Phe448Val
NM_001330589.2:c.1342T>G	NP_001317518.1:p.Phe448Val