Canonical Allele Identifier: CA1167215035

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210088T= , CM000663.2:g.53210088T=	GRCh38
NC_000001.10:g.53675760T= , CM000663.1:g.53675760T=	GRCh37
NC_000001.9:g.53448348T=	NCBI36
NG_008035.1:g.18660T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.414T= MANE Select	ENSP00000360541.3:p.Asn138=
ENST00000635862.1:c.414T=	ENSP00000490867.1:p.Asn138=
ENST00000635888.1:c.*400T=	ENSP00000490042.1:n.*400T=
ENST00000636239.1:c.*61T=	ENSP00000490066.1:n.*61T=
ENST00000636867.1:c.414T=	ENSP00000489631.1:p.Asn138=
ENST00000636891.1:c.414T=	ENSP00000490399.1:p.Asn138=
ENST00000636935.1:c.341-3176T=	ENSP00000489757.1:n.341-3176T=
ENST00000637252.1:c.414T=	ENSP00000490492.1:p.Asn138=
ENST00000637726.1:n.2614T=
ENST00000638135.1:c.*61T=	ENSP00000489756.1:n.*61T=
ENST00000371486.3:c.414T=	ENSP00000360541.3:p.Asn138=
NM_000098.2:c.414T=	NP_000089.1:p.Asn138=
XM_005270484.1:c.414T=	XP_005270541.1:p.Asn138=
NM_001330589.1:c.414T=	NP_001317518.1:p.Asn138=
NM_000098.3:c.414T= MANE Select	NP_000089.1:p.Asn138=
NM_001330589.2:c.414T=	NP_001317518.1:p.Asn138=