Canonical Allele Identifier: CA340392131

Gene: CPT2

Linked Data

• ClinVar Variation Id: 2414056
• ClinVar RCV Id: RCV003106389
• gnomAD v4: 1-53210110-A-G
• MyVariant Identifiers: chr1:g.53675782A>G (hg19) ; chr1:g.53210110A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210110A>G , CM000663.2:g.53210110A>G	GRCh38
NC_000001.10:g.53675782A>G , CM000663.1:g.53675782A>G	GRCh37
NC_000001.9:g.53448370A>G	NCBI36
NG_008035.1:g.18682A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.436A>G MANE Select	ENSP00000360541.3:p.Asn146Asp
ENST00000635862.1:c.436A>G	ENSP00000490867.1:p.Asn146Asp
ENST00000635888.1:c.*422A>G	ENSP00000490042.1:n.*422A>G
ENST00000636239.1:c.*83A>G	ENSP00000490066.1:n.*83A>G
ENST00000636867.1:c.436A>G	ENSP00000489631.1:p.Asn146Asp
ENST00000636891.1:c.436A>G	ENSP00000490399.1:p.Asn146Asp
ENST00000636935.1:c.341-3154A>G	ENSP00000489757.1:n.341-3154A>G
ENST00000637252.1:c.436A>G	ENSP00000490492.1:p.Asn146Asp
ENST00000637726.1:n.2636A>G
ENST00000638135.1:c.*83A>G	ENSP00000489756.1:n.*83A>G
ENST00000371486.3:c.436A>G	ENSP00000360541.3:p.Asn146Asp
NM_000098.2:c.436A>G	NP_000089.1:p.Asn146Asp
XM_005270484.1:c.436A>G	XP_005270541.1:p.Asn146Asp
NM_001330589.1:c.436A>G	NP_001317518.1:p.Asn146Asp
NM_000098.3:c.436A>G MANE Select	NP_000089.1:p.Asn146Asp
NM_001330589.2:c.436A>G	NP_001317518.1:p.Asn146Asp