Canonical Allele Identifier: CA1140886541

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53213509C= , CM000663.2:g.53213509C=	GRCh38
NC_000001.10:g.53679181C= , CM000663.1:g.53679181C=	GRCh37
NC_000001.9:g.53451769C=	NCBI36
NG_008035.1:g.22081C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1891C= MANE Select	ENSP00000360541.3:p.Arg631=
ENST00000635862.1:c.1858C=	ENSP00000490867.1:p.Arg620=
ENST00000635888.1:c.*1877C=	ENSP00000490042.1:n.*1877C=
ENST00000636239.1:c.*1538C=	ENSP00000490066.1:n.*1538C=
ENST00000636867.1:c.1822C=	ENSP00000489631.1:p.Arg608=
ENST00000636891.1:c.*144C=	ENSP00000490399.1:n.*144C=
ENST00000636935.1:c.586C=	ENSP00000489757.1:p.Arg196=
ENST00000637252.1:c.1927C=	ENSP00000490492.1:p.Arg643=
ENST00000638135.1:c.*1538C=	ENSP00000489756.1:n.*1538C=
ENST00000371486.3:c.1891C=	ENSP00000360541.3:p.Arg631=
NM_000098.2:c.1891C=	NP_000089.1:p.Arg631=
XM_005270484.1:c.1822C=	XP_005270541.1:p.Arg608=
NM_001330589.1:c.1822C=	NP_001317518.1:p.Arg608=
NM_000098.3:c.1891C= MANE Select	NP_000089.1:p.Arg631=
NM_001330589.2:c.1822C=	NP_001317518.1:p.Arg608=