Canonical Allele Identifier: CA2655261576

Gene: SLC25A1

Linked Data

• gnomAD v4: 22-19177061-AGGCCCTTCCCACCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19177067_19177081del , CM000684.2:g.19177067_19177081del	GRCh38
NC_000022.10:g.19164580_19164594del , CM000684.1:g.19164580_19164594del	GRCh37
NC_000022.9:g.17544580_17544594del	NCBI36
NG_033863.1:g.6788_6802del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.526+44_526+58del MANE Select	ENSP00000215882.5:n.526+44_526+58del
ENST00000215882.9:c.526+44_526+58del	ENSP00000215882.5:n.526+44_526+58del
ENST00000451283.5:c.217+44_217+58del	ENSP00000401480.1:n.217+44_217+58del
ENST00000461267.1:n.672+44_672+58del
ENST00000470922.5:n.668+44_668+58del
NM_001256534.1:c.547+44_547+58del	NP_001243463.1:n.547+44_547+58del
NM_001287387.1:c.217+44_217+58del	NP_001274316.1:n.217+44_217+58del
NM_005984.4:c.526+44_526+58del	NP_005975.1:n.526+44_526+58del
NR_046298.2:n.577+44_577+58del
NM_005984.5:c.526+44_526+58del MANE Select	NP_005975.1:n.526+44_526+58del
NM_001256534.2:c.547+44_547+58del	NP_001243463.1:n.547+44_547+58del
NM_001287387.2:c.217+44_217+58del	NP_001274316.1:n.217+44_217+58del
NR_046298.3:n.450+44_450+58del