Canonical Allele Identifier: CA1167215182

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210463_53210464delinsTG , CM000663.2:g.53210463_53210464delinsTG	GRCh38
NC_000001.10:g.53676135_53676136delinsTG , CM000663.1:g.53676135_53676136delinsTG	GRCh37
NC_000001.9:g.53448723_53448724delinsTG	NCBI36
NG_008035.1:g.19035_19036delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.789_790delinsTG MANE Select	ENSP00000360541.3:p.Ile263=
ENST00000635862.1:c.789_790delinsTG	ENSP00000490867.1:p.Ile263=
ENST00000635888.1:c.*775_*776delinsTG	ENSP00000490042.1:n.*775_*776delinsTG
ENST00000636239.1:c.*436_*437delinsTG	ENSP00000490066.1:n.*436_*437delinsTG
ENST00000636867.1:c.789_790delinsTG	ENSP00000489631.1:p.Ile263=
ENST00000636891.1:c.789_790delinsTG	ENSP00000490399.1:p.Ile263=
ENST00000636935.1:c.341-2801_341-2800delinsTG	ENSP00000489757.1:n.341-2801_341-2800delinsTG
ENST00000637252.1:c.789_790delinsTG	ENSP00000490492.1:p.Ile263=
ENST00000637726.1:n.2989_2990delinsTG
ENST00000638135.1:c.*436_*437delinsTG	ENSP00000489756.1:n.*436_*437delinsTG
ENST00000371486.3:c.789_790delinsTG	ENSP00000360541.3:p.Ile263=
NM_000098.2:c.789_790delinsTG	NP_000089.1:p.Ile263=
XM_005270484.1:c.789_790delinsTG	XP_005270541.1:p.Ile263=
NM_001330589.1:c.789_790delinsTG	NP_001317518.1:p.Ile263=
NM_000098.3:c.789_790delinsTG MANE Select	NP_000089.1:p.Ile263=
NM_001330589.2:c.789_790delinsTG	NP_001317518.1:p.Ile263=