Canonical Allele Identifier: CA1167215235

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53210594_53210597delinsTGAG , CM000663.2:g.53210594_53210597delinsTGAG	GRCh38
NC_000001.10:g.53676266_53676269delinsTGAG , CM000663.1:g.53676266_53676269delinsTGAG	GRCh37
NC_000001.9:g.53448854_53448857delinsTGAG	NCBI36
NG_008035.1:g.19166_19169delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.920_923delinsTGAG MANE Select	ENSP00000360541.3:p.Met307=
ENST00000635862.1:c.920_923delinsTGAG	ENSP00000490867.1:p.Met307=
ENST00000635888.1:c.*906_*909delinsTGAG	ENSP00000490042.1:n.*906_*909delinsTGAG
ENST00000636239.1:c.*567_*570delinsTGAG	ENSP00000490066.1:n.*567_*570delinsTGAG
ENST00000636867.1:c.920_923delinsTGAG	ENSP00000489631.1:p.Met307=
ENST00000636891.1:c.920_923delinsTGAG	ENSP00000490399.1:p.Met307=
ENST00000636935.1:c.341-2670_341-2667delinsTGAG	ENSP00000489757.1:n.341-2670_341-2667delinsTGAG
ENST00000637252.1:c.920_923delinsTGAG	ENSP00000490492.1:p.Met307=
ENST00000637726.1:n.3120_3123delinsTGAG
ENST00000638135.1:c.*567_*570delinsTGAG	ENSP00000489756.1:n.*567_*570delinsTGAG
ENST00000371486.3:c.920_923delinsTGAG	ENSP00000360541.3:p.Met307=
NM_000098.2:c.920_923delinsTGAG	NP_000089.1:p.Met307=
XM_005270484.1:c.920_923delinsTGAG	XP_005270541.1:p.Met307=
NM_001330589.1:c.920_923delinsTGAG	NP_001317518.1:p.Met307=
NM_000098.3:c.920_923delinsTGAG MANE Select	NP_000089.1:p.Met307=
NM_001330589.2:c.920_923delinsTGAG	NP_001317518.1:p.Met307=