Canonical Allele Identifier: CA2645711359

Gene: CPT2

Linked Data

• gnomAD v4: 1-53209952-TCAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53209953_53209956del , CM000663.2:g.53209953_53209956del	GRCh38
NC_000001.10:g.53675625_53675628del , CM000663.1:g.53675625_53675628del	GRCh37
NC_000001.9:g.53448213_53448216del	NCBI36
NG_008035.1:g.18525_18528del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.4:c.341-62_341-59del MANE Select	ENSP00000360541.3:n.341-62_341-59del
ENST00000635862.1:c.341-62_341-59del	ENSP00000490867.1:n.341-62_341-59del
ENST00000635888.1:c.*327-62_*327-59del	ENSP00000490042.1:n.*327-62_*327-59del
ENST00000636239.1:c.234-62_234-59del	ENSP00000490066.1:n.234-62_234-59del
ENST00000636867.1:c.341-62_341-59del	ENSP00000489631.1:n.341-62_341-59del
ENST00000636891.1:c.341-62_341-59del	ENSP00000490399.1:n.341-62_341-59del
ENST00000636935.1:c.341-3311_341-3308del	ENSP00000489757.1:n.341-3311_341-3308del
ENST00000637252.1:c.341-62_341-59del	ENSP00000490492.1:n.341-62_341-59del
ENST00000637726.1:n.2479_2482del
ENST00000638135.1:c.153-62_153-59del	ENSP00000489756.1:n.153-62_153-59del
ENST00000371486.3:c.341-62_341-59del	ENSP00000360541.3:n.341-62_341-59del
NM_000098.2:c.341-62_341-59del	NP_000089.1:n.341-62_341-59del
XM_005270484.1:c.341-62_341-59del	XP_005270541.1:n.341-62_341-59del
NM_001330589.1:c.341-62_341-59del	NP_001317518.1:n.341-62_341-59del
NM_000098.3:c.341-62_341-59del MANE Select	NP_000089.1:n.341-62_341-59del
NM_001330589.2:c.341-62_341-59del	NP_001317518.1:n.341-62_341-59del