Canonical Allele Identifier: CA2655261314

Gene: SLC25A1

Linked Data

• gnomAD v4: 22-19176090-TGGCGGTGCCTGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176097_19176108del , CM000684.2:g.19176097_19176108del	GRCh38
NC_000022.10:g.19163610_19163621del , CM000684.1:g.19163610_19163621del	GRCh37
NC_000022.9:g.17543610_17543621del	NCBI36
NG_033863.1:g.7762_7773del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.*28_*39del MANE Select	ENSP00000215882.5:n.*28_*39del
ENST00000215882.9:c.*28_*39del	ENSP00000215882.5:n.*28_*39del
ENST00000451283.5:c.*28_*39del	ENSP00000401480.1:n.*28_*39del
ENST00000470922.5:n.1106_1117del
NM_001256534.1:c.*28_*39del	NP_001243463.1:n.*28_*39del
NM_001287387.1:c.*28_*39del	NP_001274316.1:n.*28_*39del
NM_005984.4:c.*28_*39del	NP_005975.1:n.*28_*39del
NR_046298.2:n.1015_1026del
NM_005984.5:c.*28_*39del MANE Select	NP_005975.1:n.*28_*39del
NM_001256534.2:c.*28_*39del	NP_001243463.1:n.*28_*39del
NM_001287387.2:c.*28_*39del	NP_001274316.1:n.*28_*39del
NR_046298.3:n.888_899del