Canonical Allele Identifier: CA844156083

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1309274595
• gnomAD v3: 7-96121502-GT-G
• gnomAD v4: 7-96121502-GT-G
• MyVariant Identifiers: chr7:g.95750815del (hg19) ; chr7:g.96121503del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121504del , CM000669.2:g.96121504del	GRCh38
NC_000007.13:g.95750816del , CM000669.1:g.95750816del	GRCh37
NC_000007.12:g.95588752del	NCBI36
NG_012247.1:g.205645del
NG_012247.2:g.205645del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1842-126del MANE Select	ENSP00000265631.6:n.1842-126del
ENST00000265631.9:c.1842-126del	ENSP00000265631.5:n.1842-126del
ENST00000416240.6:c.1845-126del	ENSP00000400101.2:n.1845-126del
ENST00000494085.1:n.345-126del
NM_001160210.1:c.1845-126del	NP_001153682.1:n.1845-126del
NM_014251.2:c.1842-126del	NP_055066.1:n.1842-126del
NR_027662.1:n.1917-126del
XM_006715831.2:c.1875-126del	XP_006715894.1:n.1875-126del
XM_011515728.1:c.990-126del	XP_011514030.1:n.990-126del
XM_006715831.4:c.1875-126del	XP_006715894.1:n.1875-126del
XM_017011663.1:c.1833-126del	XP_016867152.1:n.1833-126del
XM_017011664.2:c.990-126del	XP_016867153.1:n.990-126del
XM_017011665.1:c.990-126del	XP_016867154.1:n.990-126del
XR_001744525.2:n.2088-126del
XR_002956405.1:n.2646-126del
NM_014251.3:c.1842-126del MANE Select	NP_055066.1:n.1842-126del
NR_027662.2:n.1868-126del
NM_001160210.2:c.1845-126del	NP_001153682.1:n.1845-126del