Canonical Allele Identifier: CA1167215216

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210551_53210553delinsAGT , CM000663.2:g.53210551_53210553delinsAGT	GRCh38
NC_000001.10:g.53676223_53676225delinsAGT , CM000663.1:g.53676223_53676225delinsAGT	GRCh37
NC_000001.9:g.53448811_53448813delinsAGT	NCBI36
NG_008035.1:g.19123_19125delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.877_879delinsAGT MANE Select	ENSP00000360541.3:p.Ser293=
ENST00000635862.1:c.877_879delinsAGT	ENSP00000490867.1:p.Ser293=
ENST00000635888.1:c.*863_*865delinsAGT	ENSP00000490042.1:n.*863_*865delinsAGT
ENST00000636239.1:c.*524_*526delinsAGT	ENSP00000490066.1:n.*524_*526delinsAGT
ENST00000636867.1:c.877_879delinsAGT	ENSP00000489631.1:p.Ser293=
ENST00000636891.1:c.877_879delinsAGT	ENSP00000490399.1:p.Ser293=
ENST00000636935.1:c.341-2713_341-2711delinsAGT	ENSP00000489757.1:n.341-2713_341-2711delinsAGT
ENST00000637252.1:c.877_879delinsAGT	ENSP00000490492.1:p.Ser293=
ENST00000637726.1:n.3077_3079delinsAGT
ENST00000638135.1:c.*524_*526delinsAGT	ENSP00000489756.1:n.*524_*526delinsAGT
ENST00000371486.3:c.877_879delinsAGT	ENSP00000360541.3:p.Ser293=
NM_000098.2:c.877_879delinsAGT	NP_000089.1:p.Ser293=
XM_005270484.1:c.877_879delinsAGT	XP_005270541.1:p.Ser293=
NM_001330589.1:c.877_879delinsAGT	NP_001317518.1:p.Ser293=
NM_000098.3:c.877_879delinsAGT MANE Select	NP_000089.1:p.Ser293=
NM_001330589.2:c.877_879delinsAGT	NP_001317518.1:p.Ser293=