Canonical Allele Identifier: CA1140886534

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53202427C= , CM000663.2:g.53202427C=	GRCh38
NC_000001.10:g.53668099C= , CM000663.1:g.53668099C=	GRCh37
NC_000001.9:g.53440687C=	NCBI36
NG_008035.1:g.10999C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.338C= MANE Select	ENSP00000360541.3:p.Ser113=
ENST00000468572.2:n.423C=
ENST00000635862.1:c.338C=	ENSP00000490867.1:p.Ser113=
ENST00000635888.1:c.*324C=	ENSP00000490042.1:n.*324C=
ENST00000636239.1:c.233+1628C=	ENSP00000490066.1:n.233+1628C=
ENST00000636673.1:n.2651C=
ENST00000636867.1:c.338C=	ENSP00000489631.1:p.Ser113=
ENST00000636891.1:c.338C=	ENSP00000490399.1:p.Ser113=
ENST00000636935.1:c.338C=	ENSP00000489757.1:p.Ser113=
ENST00000637252.1:c.338C=	ENSP00000490492.1:p.Ser113=
ENST00000638135.1:c.152+5332C=	ENSP00000489756.1:n.152+5332C=
ENST00000371486.3:c.338C=	ENSP00000360541.3:p.Ser113=
ENST00000468572.1:n.423C=
NM_000098.2:c.338C=	NP_000089.1:p.Ser113=
XM_005270484.1:c.338C=	XP_005270541.1:p.Ser113=
NM_001330589.1:c.338C=	NP_001317518.1:p.Ser113=
NM_000098.3:c.338C= MANE Select	NP_000089.1:p.Ser113=
NM_001330589.2:c.338C=	NP_001317518.1:p.Ser113=