Canonical Allele Identifier: CA1140495625

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53213275G= , CM000663.2:g.53213275G=	GRCh38
NC_000001.10:g.53678947G= , CM000663.1:g.53678947G=	GRCh37
NC_000001.9:g.53451535G=	NCBI36
NG_008035.1:g.21847G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1657G= MANE Select	ENSP00000360541.3:p.Asp553=
ENST00000635862.1:c.1624G=	ENSP00000490867.1:p.Asp542=
ENST00000635888.1:c.*1643G=	ENSP00000490042.1:n.*1643G=
ENST00000636239.1:c.*1304G=	ENSP00000490066.1:n.*1304G=
ENST00000636867.1:c.1588G=	ENSP00000489631.1:p.Asp530=
ENST00000636891.1:c.1707G=	ENSP00000490399.1:p.Leu569=
ENST00000636935.1:c.352G=	ENSP00000489757.1:p.Asp118=
ENST00000637252.1:c.1693G=	ENSP00000490492.1:p.Asp565=
ENST00000638135.1:c.*1304G=	ENSP00000489756.1:n.*1304G=
ENST00000371486.3:c.1657G=	ENSP00000360541.3:p.Asp553=
NM_000098.2:c.1657G=	NP_000089.1:p.Asp553=
XM_005270484.1:c.1588G=	XP_005270541.1:p.Asp530=
NM_001330589.1:c.1588G=	NP_001317518.1:p.Asp530=
NM_000098.3:c.1657G= MANE Select	NP_000089.1:p.Asp553=
NM_001330589.2:c.1588G=	NP_001317518.1:p.Asp530=