Canonical Allele Identifier: CA1143666365

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210090C= , CM000663.2:g.53210090C=	GRCh38
NC_000001.10:g.53675762C= , CM000663.1:g.53675762C=	GRCh37
NC_000001.9:g.53448350C=	NCBI36
NG_008035.1:g.18662C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.416C= MANE Select	ENSP00000360541.3:p.Pro139=
ENST00000635862.1:c.416C=	ENSP00000490867.1:p.Pro139=
ENST00000635888.1:c.*402C=	ENSP00000490042.1:n.*402C=
ENST00000636239.1:c.*63C=	ENSP00000490066.1:n.*63C=
ENST00000636867.1:c.416C=	ENSP00000489631.1:p.Pro139=
ENST00000636891.1:c.416C=	ENSP00000490399.1:p.Pro139=
ENST00000636935.1:c.341-3174C=	ENSP00000489757.1:n.341-3174C=
ENST00000637252.1:c.416C=	ENSP00000490492.1:p.Pro139=
ENST00000637726.1:n.2616C=
ENST00000638135.1:c.*63C=	ENSP00000489756.1:n.*63C=
ENST00000371486.3:c.416C=	ENSP00000360541.3:p.Pro139=
NM_000098.2:c.416C=	NP_000089.1:p.Pro139=
XM_005270484.1:c.416C=	XP_005270541.1:p.Pro139=
NM_001330589.1:c.416C=	NP_001317518.1:p.Pro139=
NM_000098.3:c.416C= MANE Select	NP_000089.1:p.Pro139=
NM_001330589.2:c.416C=	NP_001317518.1:p.Pro139=