Canonical Allele Identifier: CA1167214985

Gene: CPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53209944_53209947delinsTTTC , CM000663.2:g.53209944_53209947delinsTTTC	GRCh38
NC_000001.10:g.53675616_53675619delinsTTTC , CM000663.1:g.53675616_53675619delinsTTTC	GRCh37
NC_000001.9:g.53448204_53448207delinsTTTC	NCBI36
NG_008035.1:g.18516_18519delinsTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.341-71_341-68delinsTTTC MANE Select	ENSP00000360541.3:n.341-71_341-68delinsTTTC
ENST00000635862.1:c.341-71_341-68delinsTTTC	ENSP00000490867.1:n.341-71_341-68delinsTTTC
ENST00000635888.1:c.*327-71_*327-68delinsTTTC	ENSP00000490042.1:n.*327-71_*327-68delinsTTTC
ENST00000636239.1:c.234-71_234-68delinsTTTC	ENSP00000490066.1:n.234-71_234-68delinsTTTC
ENST00000636867.1:c.341-71_341-68delinsTTTC	ENSP00000489631.1:n.341-71_341-68delinsTTTC
ENST00000636891.1:c.341-71_341-68delinsTTTC	ENSP00000490399.1:n.341-71_341-68delinsTTTC
ENST00000636935.1:c.341-3320_341-3317delinsTTTC	ENSP00000489757.1:n.341-3320_341-3317delinsTTTC
ENST00000637252.1:c.341-71_341-68delinsTTTC	ENSP00000490492.1:n.341-71_341-68delinsTTTC
ENST00000637726.1:n.2470_2473delinsTTTC
ENST00000638135.1:c.153-71_153-68delinsTTTC	ENSP00000489756.1:n.153-71_153-68delinsTTTC
ENST00000371486.3:c.341-71_341-68delinsTTTC	ENSP00000360541.3:n.341-71_341-68delinsTTTC
NM_000098.2:c.341-71_341-68delinsTTTC	NP_000089.1:n.341-71_341-68delinsTTTC
XM_005270484.1:c.341-71_341-68delinsTTTC	XP_005270541.1:n.341-71_341-68delinsTTTC
NM_001330589.1:c.341-71_341-68delinsTTTC	NP_001317518.1:n.341-71_341-68delinsTTTC
NM_000098.3:c.341-71_341-68delinsTTTC MANE Select	NP_000089.1:n.341-71_341-68delinsTTTC
NM_001330589.2:c.341-71_341-68delinsTTTC	NP_001317518.1:n.341-71_341-68delinsTTTC