Canonical Allele Identifier: CA1167214970

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53209917_53209918delinsAT , CM000663.2:g.53209917_53209918delinsAT	GRCh38
NC_000001.10:g.53675589_53675590delinsAT , CM000663.1:g.53675589_53675590delinsAT	GRCh37
NC_000001.9:g.53448177_53448178delinsAT	NCBI36
NG_008035.1:g.18489_18490delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.341-98_341-97delinsAT MANE Select	ENSP00000360541.3:n.341-98_341-97delinsAT
ENST00000635862.1:c.341-98_341-97delinsAT	ENSP00000490867.1:n.341-98_341-97delinsAT
ENST00000635888.1:c.*327-98_*327-97delinsAT	ENSP00000490042.1:n.*327-98_*327-97delinsAT
ENST00000636239.1:c.234-98_234-97delinsAT	ENSP00000490066.1:n.234-98_234-97delinsAT
ENST00000636867.1:c.341-98_341-97delinsAT	ENSP00000489631.1:n.341-98_341-97delinsAT
ENST00000636891.1:c.341-98_341-97delinsAT	ENSP00000490399.1:n.341-98_341-97delinsAT
ENST00000636935.1:c.341-3347_341-3346delinsAT	ENSP00000489757.1:n.341-3347_341-3346delinsAT
ENST00000637252.1:c.341-98_341-97delinsAT	ENSP00000490492.1:n.341-98_341-97delinsAT
ENST00000637726.1:n.2443_2444delinsAT
ENST00000638135.1:c.153-98_153-97delinsAT	ENSP00000489756.1:n.153-98_153-97delinsAT
ENST00000371486.3:c.341-98_341-97delinsAT	ENSP00000360541.3:n.341-98_341-97delinsAT
NM_000098.2:c.341-98_341-97delinsAT	NP_000089.1:n.341-98_341-97delinsAT
XM_005270484.1:c.341-98_341-97delinsAT	XP_005270541.1:n.341-98_341-97delinsAT
NM_001330589.1:c.341-98_341-97delinsAT	NP_001317518.1:n.341-98_341-97delinsAT
NM_000098.3:c.341-98_341-97delinsAT MANE Select	NP_000089.1:n.341-98_341-97delinsAT
NM_001330589.2:c.341-98_341-97delinsAT	NP_001317518.1:n.341-98_341-97delinsAT