Canonical Allele Identifier: CA2645707604

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53200708T>C , CM000663.2:g.53200708T>C	GRCh38
NC_000001.10:g.53666380T>C , CM000663.1:g.53666380T>C	GRCh37
NC_000001.9:g.53438968T>C	NCBI36
NG_008035.1:g.9280T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.153-11T>C MANE Select	ENSP00000360541.3:n.153-11T>C
ENST00000468572.2:n.238-11T>C
ENST00000635862.1:c.153-11T>C	ENSP00000490867.1:n.153-11T>C
ENST00000635888.1:c.*139-11T>C	ENSP00000490042.1:n.*139-11T>C
ENST00000636239.1:c.153-11T>C	ENSP00000490066.1:n.153-11T>C
ENST00000636673.1:n.932T>C
ENST00000636867.1:c.153-11T>C	ENSP00000489631.1:n.153-11T>C
ENST00000636891.1:c.153-11T>C	ENSP00000490399.1:n.153-11T>C
ENST00000636935.1:c.153-11T>C	ENSP00000489757.1:n.153-11T>C
ENST00000637252.1:c.153-11T>C	ENSP00000490492.1:n.153-11T>C
ENST00000638135.1:c.152+3613T>C	ENSP00000489756.1:n.152+3613T>C
ENST00000371486.3:c.153-11T>C	ENSP00000360541.3:n.153-11T>C
ENST00000468572.1:n.238-11T>C
NM_000098.2:c.153-11T>C	NP_000089.1:n.153-11T>C
XM_005270484.1:c.153-11T>C	XP_005270541.1:n.153-11T>C
NM_001330589.1:c.153-11T>C	NP_001317518.1:n.153-11T>C
NM_000098.3:c.153-11T>C MANE Select	NP_000089.1:n.153-11T>C
NM_001330589.2:c.153-11T>C	NP_001317518.1:n.153-11T>C