Canonical Allele Identifier: CA1167215047

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210123C= , CM000663.2:g.53210123C=	GRCh38
NC_000001.10:g.53675795C= , CM000663.1:g.53675795C=	GRCh37
NC_000001.9:g.53448383C=	NCBI36
NG_008035.1:g.18695C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.449C= MANE Select	ENSP00000360541.3:p.Thr150=
ENST00000635862.1:c.449C=	ENSP00000490867.1:p.Thr150=
ENST00000635888.1:c.*435C=	ENSP00000490042.1:n.*435C=
ENST00000636239.1:c.*96C=	ENSP00000490066.1:n.*96C=
ENST00000636867.1:c.449C=	ENSP00000489631.1:p.Thr150=
ENST00000636891.1:c.449C=	ENSP00000490399.1:p.Thr150=
ENST00000636935.1:c.341-3141C=	ENSP00000489757.1:n.341-3141C=
ENST00000637252.1:c.449C=	ENSP00000490492.1:p.Thr150=
ENST00000637726.1:n.2649C=
ENST00000638135.1:c.*96C=	ENSP00000489756.1:n.*96C=
ENST00000371486.3:c.449C=	ENSP00000360541.3:p.Thr150=
NM_000098.2:c.449C=	NP_000089.1:p.Thr150=
XM_005270484.1:c.449C=	XP_005270541.1:p.Thr150=
NM_001330589.1:c.449C=	NP_001317518.1:p.Thr150=
NM_000098.3:c.449C= MANE Select	NP_000089.1:p.Thr150=
NM_001330589.2:c.449C=	NP_001317518.1:p.Thr150=