Canonical Allele Identifier: CA4352761

Gene: SLC25A13

Linked Data

• dbSNP Id: rs766856931
• ExAC: 7:95750722 AT / A
• gnomAD v2: 7-95750722-AT-A
• gnomAD v3: 7-96121410-AT-A
• gnomAD v4: 7-96121410-AT-A
• MyVariant Identifiers: chr7:g.95750723del (hg19) ; chr7:g.96121411del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121416del , CM000669.2:g.96121416del	GRCh38
NC_000007.13:g.95750728del , CM000669.1:g.95750728del	GRCh37
NC_000007.12:g.95588664del	NCBI36
NG_012247.1:g.205737del
NG_012247.2:g.205737del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1842-34del MANE Select	ENSP00000265631.6:n.1842-34del
ENST00000265631.9:c.1842-34del	ENSP00000265631.5:n.1842-34del
ENST00000416240.6:c.1845-34del	ENSP00000400101.2:n.1845-34del
ENST00000494085.1:n.345-34del
NM_001160210.1:c.1845-34del	NP_001153682.1:n.1845-34del
NM_014251.2:c.1842-34del	NP_055066.1:n.1842-34del
NR_027662.1:n.1917-34del
XM_006715831.2:c.1875-34del	XP_006715894.1:n.1875-34del
XM_011515728.1:c.990-34del	XP_011514030.1:n.990-34del
XM_006715831.4:c.1875-34del	XP_006715894.1:n.1875-34del
XM_017011663.1:c.1833-34del	XP_016867152.1:n.1833-34del
XM_017011664.2:c.990-34del	XP_016867153.1:n.990-34del
XM_017011665.1:c.990-34del	XP_016867154.1:n.990-34del
XR_001744525.2:n.2088-34del
XR_002956405.1:n.2646-34del
NM_014251.3:c.1842-34del MANE Select	NP_055066.1:n.1842-34del
NR_027662.2:n.1868-34del
NM_001160210.2:c.1845-34del	NP_001153682.1:n.1845-34del