Canonical Allele Identifier: CA1167208943

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53196910_53196924delinsTGCCGCGTTCTCGCC , CM000663.2:g.53196910_53196924delinsTGCCGCGTTCTCGCC	GRCh38
NC_000001.10:g.53662582_53662596delinsTGCCGCGTTCTCGCC , CM000663.1:g.53662582_53662596delinsTGCCGCGTTCTCGCC	GRCh37
NC_000001.9:g.53435170_53435184delinsTGCCGCGTTCTCGCC	NCBI36
NG_008035.1:g.5482_5496delinsTGCCGCGTTCTCGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000371486.4:c.-34_-20delinsTGCCGCGTTCTCGCC MANE Select	ENSP00000360541.3:n.-34_-20delinsTGCCGCGT...
ENST00000468572.2:n.52_66delinsTGCCGCGTTCTCGCC
ENST00000635862.1:c.-34_-20delinsTGCCGCGTTCTCGCC	ENSP00000490867.1:n.-34_-20delinsTGCCGCGT...
ENST00000635888.1:c.-34_-20delinsTGCCGCGTTCTCGCC	ENSP00000490042.1:n.-34_-20delinsTGCCGCGT...
ENST00000636239.1:c.-34_-20delinsTGCCGCGTTCTCGCC	ENSP00000490066.1:n.-34_-20delinsTGCCGCGT...
ENST00000636867.1:c.-34_-20delinsTGCCGCGTTCTCGCC	ENSP00000489631.1:n.-34_-20delinsTGCCGCGT...
ENST00000636891.1:c.-34_-20delinsTGCCGCGTTCTCGCC	ENSP00000490399.1:n.-34_-20delinsTGCCGCGT...
ENST00000636935.1:c.-34_-20delinsTGCCGCGTTCTCGCC	ENSP00000489757.1:n.-34_-20delinsTGCCGCGT...
ENST00000637252.1:c.-34_-20delinsTGCCGCGTTCTCGCC	ENSP00000490492.1:n.-34_-20delinsTGCCGCGT...
ENST00000638135.1:c.-34_-20delinsTGCCGCGTTCTCGCC	ENSP00000489756.1:n.-34_-20delinsTGCCGCGT...
ENST00000371486.3:c.-34_-20delinsTGCCGCGTTCTCGCC	ENSP00000360541.3:n.-34_-20delinsTGCCGCGT...
ENST00000468572.1:n.52_66delinsTGCCGCGTTCTCGCC
NM_000098.2:c.-34_-20delinsTGCCGCGTTCTCGCC	NP_000089.1:n.-34_-20delinsTGCCGCGTTCTCGC...
XM_005270484.1:c.-34_-20delinsTGCCGCGTTCTCGCC	XP_005270541.1:n.-34_-20delinsTGCCGCGTTCT...
NM_001330589.1:c.-34_-20delinsTGCCGCGTTCTCGCC	NP_001317518.1:n.-34_-20delinsTGCCGCGTTCT...
NM_000098.3:c.-34_-20delinsTGCCGCGTTCTCGCC MANE Select	NP_000089.1:n.-34_-20delinsTGCCGCGTTCTCGC...
NM_001330589.2:c.-34_-20delinsTGCCGCGTTCTCGCC	NP_001317518.1:n.-34_-20delinsTGCCGCGTTCT...