Canonical Allele Identifier: CA1167208928

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53196892A= , CM000663.2:g.53196892A=	GRCh38
NC_000001.10:g.53662564A= , CM000663.1:g.53662564A=	GRCh37
NC_000001.9:g.53435152A=	NCBI36
NG_008035.1:g.5464A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371486.4:c.-52A= MANE Select	ENSP00000360541.3:n.-52A=
ENST00000468572.2:n.34A=
ENST00000635862.1:c.-52A=	ENSP00000490867.1:n.-52A=
ENST00000635888.1:c.-52A=	ENSP00000490042.1:n.-52A=
ENST00000636239.1:c.-52A=	ENSP00000490066.1:n.-52A=
ENST00000636867.1:c.-52A=	ENSP00000489631.1:n.-52A=
ENST00000636891.1:c.-52A=	ENSP00000490399.1:n.-52A=
ENST00000636935.1:c.-52A=	ENSP00000489757.1:n.-52A=
ENST00000637252.1:c.-52A=	ENSP00000490492.1:n.-52A=
ENST00000371486.3:c.-52A=	ENSP00000360541.3:n.-52A=
ENST00000468572.1:n.34A=
NM_000098.2:c.-52A=	NP_000089.1:n.-52A=
XM_005270484.1:c.-52A=	XP_005270541.1:n.-52A=
NM_001330589.1:c.-52A=	NP_001317518.1:n.-52A=
NM_000098.3:c.-52A= MANE Select	NP_000089.1:n.-52A=
NM_001330589.2:c.-52A=	NP_001317518.1:n.-52A=