Canonical Allele Identifier: CA1167216261

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53213182T= , CM000663.2:g.53213182T=	GRCh38
NC_000001.10:g.53678854T= , CM000663.1:g.53678854T=	GRCh37
NC_000001.9:g.53451442T=	NCBI36
NG_008035.1:g.21754T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1646-82T= MANE Select	ENSP00000360541.3:n.1646-82T=
ENST00000635862.1:c.1613-82T=	ENSP00000490867.1:n.1613-82T=
ENST00000635888.1:c.*1632-82T=	ENSP00000490042.1:n.*1632-82T=
ENST00000636239.1:c.*1293-82T=	ENSP00000490066.1:n.*1293-82T=
ENST00000636867.1:c.1577-82T=	ENSP00000489631.1:n.1577-82T=
ENST00000636891.1:c.1696-82T=	ENSP00000490399.1:n.1696-82T=
ENST00000636935.1:c.341-82T=	ENSP00000489757.1:n.341-82T=
ENST00000637252.1:c.1682-82T=	ENSP00000490492.1:n.1682-82T=
ENST00000638135.1:c.*1293-82T=	ENSP00000489756.1:n.*1293-82T=
ENST00000371486.3:c.1646-82T=	ENSP00000360541.3:n.1646-82T=
NM_000098.2:c.1646-82T=	NP_000089.1:n.1646-82T=
XM_005270484.1:c.1577-82T=	XP_005270541.1:n.1577-82T=
NM_001330589.1:c.1577-82T=	NP_001317518.1:n.1577-82T=
NM_000098.3:c.1646-82T= MANE Select	NP_000089.1:n.1646-82T=
NM_001330589.2:c.1577-82T=	NP_001317518.1:n.1577-82T=