Canonical Allele Identifier: CA22626436

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53197041del , CM000663.2:g.53197041del	GRCh38
NC_000001.10:g.53662713del , CM000663.1:g.53662713del	GRCh37
NC_000001.9:g.53435301del	NCBI36
NG_008035.1:g.5613del

Transcript Alleles

HGVS	Amino-acid Change
NM_000098.3:c.98del MANE Select	NP_000089.1:p.Gln33ArgfsTer?
ENST00000371486.4:c.98del MANE Select	ENSP00000360541.3:p.Gln33ArgfsTer?
NM_000098.2:c.98del	NP_000089.1:p.Gln33ArgfsTer?
NM_001330589.1:c.98del	NP_001317518.1:p.Gln33ArgfsTer?
NM_001330589.2:c.98del	NP_001317518.1:p.Gln33ArgfsTer?
ENST00000371486.3:c.98del	ENSP00000360541.3:p.Gln33ArgfsTer?
ENST00000468572.1:n.183del
ENST00000468572.2:n.183del
ENST00000635862.1:c.98del	ENSP00000490867.1:p.Gln33ArgfsTer?
ENST00000635888.1:c.98del	ENSP00000490042.1:p.Gln33ArgfsTer30
ENST00000636239.1:c.98del	ENSP00000490066.1:p.Gln33ArgfsTer?
ENST00000636867.1:c.98del	ENSP00000489631.1:p.Gln33ArgfsTer?
ENST00000636891.1:c.98del	ENSP00000490399.1:p.Gln33ArgfsTer?
ENST00000636935.1:c.98del	ENSP00000489757.1:p.Gln33ArgfsTer?
ENST00000637252.1:c.98del	ENSP00000490492.1:p.Gln33ArgfsTer?
ENST00000638135.1:c.98del	ENSP00000489756.1:p.Gln33ArgfsTer?
XM_005270484.1:c.98del	XP_005270541.1:p.Gln33ArgfsTer?