Canonical Allele Identifier: CA22639139

Gene: CPT2

Linked Data

• dbSNP Id: rs757979320
• MyVariant Identifiers: chr1:g.53676466_53676467insG (hg19) ; chr1:g.53210794_53210795insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210798dup , CM000663.2:g.53210798dup	GRCh38
NC_000001.10:g.53676470dup , CM000663.1:g.53676470dup	GRCh37
NC_000001.9:g.53449058dup	NCBI36
NG_008035.1:g.19370dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1124dup MANE Select	ENSP00000360541.3:p.Asp376Ter
ENST00000635862.1:c.1124dup	ENSP00000490867.1:p.Asp376Ter
ENST00000635888.1:c.*1110dup	ENSP00000490042.1:n.*1110dup
ENST00000636239.1:c.*771dup	ENSP00000490066.1:n.*771dup
ENST00000636867.1:c.1124dup	ENSP00000489631.1:p.Asp376Ter
ENST00000636891.1:c.1124dup	ENSP00000490399.1:p.Asp376Ter
ENST00000636935.1:c.341-2466dup	ENSP00000489757.1:n.341-2466dup
ENST00000637252.1:c.1124dup	ENSP00000490492.1:p.Asp376Ter
ENST00000637726.1:n.3324dup
ENST00000638135.1:c.*771dup	ENSP00000489756.1:n.*771dup
ENST00000371486.3:c.1124dup	ENSP00000360541.3:p.Asp376Ter
NM_000098.2:c.1124dup	NP_000089.1:p.Asp376Ter
XM_005270484.1:c.1124dup	XP_005270541.1:p.Asp376Ter
NM_001330589.1:c.1124dup	NP_001317518.1:p.Asp376Ter
NM_000098.3:c.1124dup MANE Select	NP_000089.1:p.Asp376Ter
NM_001330589.2:c.1124dup	NP_001317518.1:p.Asp376Ter