Canonical Allele Identifier: CA2395758349

Gene: SLC25A1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19176705_19176706delinsAG , CM000684.2:g.19176705_19176706delinsAG	GRCh38
NC_000022.10:g.19164218_19164219delinsAG , CM000684.1:g.19164218_19164219delinsAG	GRCh37
NC_000022.9:g.17544218_17544219delinsAG	NCBI36
NG_033863.1:g.7158_7159delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215882.10:c.632-13_632-12delinsCT MANE Select	ENSP00000215882.5:n.632-13_632-12delinsCT
ENST00000215882.9:c.632-13_632-12delinsCT	ENSP00000215882.5:n.632-13_632-12delinsCT
ENST00000451283.5:c.323-13_323-12delinsCT	ENSP00000401480.1:n.323-13_323-12delinsCT
ENST00000461267.1:n.778-13_778-12delinsCT
ENST00000470922.5:n.774-13_774-12delinsCT
NM_001256534.1:c.653-13_653-12delinsCT	NP_001243463.1:n.653-13_653-12delinsCT
NM_001287387.1:c.323-13_323-12delinsCT	NP_001274316.1:n.323-13_323-12delinsCT
NM_005984.4:c.632-13_632-12delinsCT	NP_005975.1:n.632-13_632-12delinsCT
NR_046298.2:n.683-13_683-12delinsCT
NM_005984.5:c.632-13_632-12delinsCT MANE Select	NP_005975.1:n.632-13_632-12delinsCT
NM_001256534.2:c.653-13_653-12delinsCT	NP_001243463.1:n.653-13_653-12delinsCT
NM_001287387.2:c.323-13_323-12delinsCT	NP_001274316.1:n.323-13_323-12delinsCT
NR_046298.3:n.556-13_556-12delinsCT