Canonical Allele Identifier: CA1167215391

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53211030_53211034delinsCAAAG , CM000663.2:g.53211030_53211034delinsCAAAG	GRCh38
NC_000001.10:g.53676702_53676706delinsCAAAG , CM000663.1:g.53676702_53676706delinsCAAAG	GRCh37
NC_000001.9:g.53449290_53449294delinsCAAAG	NCBI36
NG_008035.1:g.19602_19606delinsCAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.1356_1360delinsCAAAG MANE Select	ENSP00000360541.3:p.Gly452=
ENST00000635862.1:c.1356_1360delinsCAAAG	ENSP00000490867.1:p.Gly452=
ENST00000635888.1:c.*1342_*1346delinsCAAAG	ENSP00000490042.1:n.*1342_*1346delinsCAAAG
ENST00000636239.1:c.*1003_*1007delinsCAAAG	ENSP00000490066.1:n.*1003_*1007delinsCAAAG
ENST00000636867.1:c.1356_1360delinsCAAAG	ENSP00000489631.1:p.Gly452=
ENST00000636891.1:c.1356_1360delinsCAAAG	ENSP00000490399.1:p.Gly452=
ENST00000636935.1:c.341-2234_341-2230delinsCAAAG	ENSP00000489757.1:n.341-2234_341-2230delinsCAAAG
ENST00000637252.1:c.1356_1360delinsCAAAG	ENSP00000490492.1:p.Gly452=
ENST00000637726.1:n.3556_3560delinsCAAAG
ENST00000638135.1:c.*1003_*1007delinsCAAAG	ENSP00000489756.1:n.*1003_*1007delinsCAAAG
ENST00000371486.3:c.1356_1360delinsCAAAG	ENSP00000360541.3:p.Gly452=
NM_000098.2:c.1356_1360delinsCAAAG	NP_000089.1:p.Gly452=
XM_005270484.1:c.1356_1360delinsCAAAG	XP_005270541.1:p.Gly452=
NM_001330589.1:c.1356_1360delinsCAAAG	NP_001317518.1:p.Gly452=
NM_000098.3:c.1356_1360delinsCAAAG MANE Select	NP_000089.1:p.Gly452=
NM_001330589.2:c.1356_1360delinsCAAAG	NP_001317518.1:p.Gly452=