Canonical Allele Identifier: CA1167208704

Gene: CPT2

Linked Data

• dbSNP Id: rs746815144
• gnomAD v4: 1-53196586-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53196595_53196596del , CM000663.2:g.53196595_53196596del	GRCh38
NC_000001.10:g.53662267_53662268del , CM000663.1:g.53662267_53662268del	GRCh37
NC_000001.9:g.53434855_53434856del	NCBI36
NG_008035.1:g.5167_5168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.3:c.-349_-348del	ENSP00000360541.3:n.-349_-348del
NM_000098.2:c.-349_-348del	NP_000089.1:n.-349_-348del
NM_001330589.1:c.-349_-348del	NP_001317518.1:n.-349_-348del