Canonical Allele Identifier: CA2655261585

Gene: SLC25A1

Linked Data

• gnomAD v4: 22-19177078-G-GCCCAGGTCCCTGAGCCCTATC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177079_19177099dup , CM000684.2:g.19177079_19177099dup	GRCh38
NC_000022.10:g.19164592_19164612dup , CM000684.1:g.19164592_19164612dup	GRCh37
NC_000022.9:g.17544592_17544612dup	NCBI36
NG_033863.1:g.6765_6785dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.526+21_526+41dup MANE Select	ENSP00000215882.5:n.526+21_526+41dup
ENST00000215882.9:c.526+21_526+41dup	ENSP00000215882.5:n.526+21_526+41dup
ENST00000451283.5:c.217+21_217+41dup	ENSP00000401480.1:n.217+21_217+41dup
ENST00000461267.1:n.672+21_672+41dup
ENST00000470922.5:n.668+21_668+41dup
NM_001256534.1:c.547+21_547+41dup	NP_001243463.1:n.547+21_547+41dup
NM_001287387.1:c.217+21_217+41dup	NP_001274316.1:n.217+21_217+41dup
NM_005984.4:c.526+21_526+41dup	NP_005975.1:n.526+21_526+41dup
NR_046298.2:n.577+21_577+41dup
NM_005984.5:c.526+21_526+41dup MANE Select	NP_005975.1:n.526+21_526+41dup
NM_001256534.2:c.547+21_547+41dup	NP_001243463.1:n.547+21_547+41dup
NM_001287387.2:c.217+21_217+41dup	NP_001274316.1:n.217+21_217+41dup
NR_046298.3:n.450+21_450+41dup