Canonical Allele Identifier: CA1167215070

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210197G= , CM000663.2:g.53210197G=	GRCh38
NC_000001.10:g.53675869G= , CM000663.1:g.53675869G=	GRCh37
NC_000001.9:g.53448457G=	NCBI36
NG_008035.1:g.18769G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.523G= MANE Select	ENSP00000360541.3:p.Val175=
ENST00000635862.1:c.523G=	ENSP00000490867.1:p.Val175=
ENST00000635888.1:c.*509G=	ENSP00000490042.1:n.*509G=
ENST00000636239.1:c.*170G=	ENSP00000490066.1:n.*170G=
ENST00000636867.1:c.523G=	ENSP00000489631.1:p.Val175=
ENST00000636891.1:c.523G=	ENSP00000490399.1:p.Val175=
ENST00000636935.1:c.341-3067G=	ENSP00000489757.1:n.341-3067G=
ENST00000637252.1:c.523G=	ENSP00000490492.1:p.Val175=
ENST00000637726.1:n.2723G=
ENST00000638135.1:c.*170G=	ENSP00000489756.1:n.*170G=
ENST00000371486.3:c.523G=	ENSP00000360541.3:p.Val175=
NM_000098.2:c.523G=	NP_000089.1:p.Val175=
XM_005270484.1:c.523G=	XP_005270541.1:p.Val175=
NM_001330589.1:c.523G=	NP_001317518.1:p.Val175=
NM_000098.3:c.523G= MANE Select	NP_000089.1:p.Val175=
NM_001330589.2:c.523G=	NP_001317518.1:p.Val175=