Canonical Allele Identifier: CA2655261442

Gene: SLC25A1

Linked Data

• gnomAD v4: 22-19176507-TCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176511_19176513del , CM000684.2:g.19176511_19176513del	GRCh38
NC_000022.10:g.19164024_19164026del , CM000684.1:g.19164024_19164026del	GRCh37
NC_000022.9:g.17544024_17544026del	NCBI36
NG_033863.1:g.7354_7356del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.748-16_748-14del MANE Select	ENSP00000215882.5:n.748-16_748-14del
ENST00000215882.9:c.748-16_748-14del	ENSP00000215882.5:n.748-16_748-14del
ENST00000451283.5:c.439-16_439-14del	ENSP00000401480.1:n.439-16_439-14del
ENST00000470922.5:n.890-16_890-14del
NM_001256534.1:c.769-16_769-14del	NP_001243463.1:n.769-16_769-14del
NM_001287387.1:c.439-16_439-14del	NP_001274316.1:n.439-16_439-14del
NM_005984.4:c.748-16_748-14del	NP_005975.1:n.748-16_748-14del
NR_046298.2:n.799-16_799-14del
NM_005984.5:c.748-16_748-14del MANE Select	NP_005975.1:n.748-16_748-14del
NM_001256534.2:c.769-16_769-14del	NP_001243463.1:n.769-16_769-14del
NM_001287387.2:c.439-16_439-14del	NP_001274316.1:n.439-16_439-14del
NR_046298.3:n.672-16_672-14del