Canonical Allele Identifier: CA2655261493

Gene: SLC25A1

Linked Data

• gnomAD v4: 22-19176761-TGGGTGCCCGCCACCCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176767_19176783del , CM000684.2:g.19176767_19176783del	GRCh38
NC_000022.10:g.19164280_19164296del , CM000684.1:g.19164280_19164296del	GRCh37
NC_000022.9:g.17544280_17544296del	NCBI36
NG_033863.1:g.7086_7102del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.631+68_632-69del MANE Select	ENSP00000215882.5:n.631+68_632-69del
ENST00000215882.9:c.631+68_632-69del	ENSP00000215882.5:n.631+68_632-69del
ENST00000451283.5:c.322+68_323-69del	ENSP00000401480.1:n.322+68_323-69del
ENST00000461267.1:n.777+68_778-69del
ENST00000470922.5:n.773+68_774-69del
NM_001256534.1:c.652+68_653-69del	NP_001243463.1:n.652+68_653-69del
NM_001287387.1:c.322+68_323-69del	NP_001274316.1:n.322+68_323-69del
NM_005984.4:c.631+68_632-69del	NP_005975.1:n.631+68_632-69del
NR_046298.2:n.682+68_683-69del
NM_005984.5:c.631+68_632-69del MANE Select	NP_005975.1:n.631+68_632-69del
NM_001256534.2:c.652+68_653-69del	NP_001243463.1:n.652+68_653-69del
NM_001287387.2:c.322+68_323-69del	NP_001274316.1:n.322+68_323-69del
NR_046298.3:n.555+68_556-69del