Canonical Allele Identifier: CA2574373968

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53213185T>G , CM000663.2:g.53213185T>G	GRCh38
NC_000001.10:g.53678857T>G , CM000663.1:g.53678857T>G	GRCh37
NC_000001.9:g.53451445T>G	NCBI36
NG_008035.1:g.21757T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1646-79T>G MANE Select	ENSP00000360541.3:n.1646-79T>G
ENST00000635862.1:c.1613-79T>G	ENSP00000490867.1:n.1613-79T>G
ENST00000635888.1:c.*1632-79T>G	ENSP00000490042.1:n.*1632-79T>G
ENST00000636239.1:c.*1293-79T>G	ENSP00000490066.1:n.*1293-79T>G
ENST00000636867.1:c.1577-79T>G	ENSP00000489631.1:n.1577-79T>G
ENST00000636891.1:c.1696-79T>G	ENSP00000490399.1:n.1696-79T>G
ENST00000636935.1:c.341-79T>G	ENSP00000489757.1:n.341-79T>G
ENST00000637252.1:c.1682-79T>G	ENSP00000490492.1:n.1682-79T>G
ENST00000638135.1:c.*1293-79T>G	ENSP00000489756.1:n.*1293-79T>G
ENST00000371486.3:c.1646-79T>G	ENSP00000360541.3:n.1646-79T>G
NM_000098.2:c.1646-79T>G	NP_000089.1:n.1646-79T>G
XM_005270484.1:c.1577-79T>G	XP_005270541.1:n.1577-79T>G
NM_001330589.1:c.1577-79T>G	NP_001317518.1:n.1577-79T>G
NM_000098.3:c.1646-79T>G MANE Select	NP_000089.1:n.1646-79T>G
NM_001330589.2:c.1577-79T>G	NP_001317518.1:n.1577-79T>G