Canonical Allele Identifier: CA1104711958

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1794527032
• gnomAD v3: 7-96184083-AT-A
• gnomAD v4: 7-96184083-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184087del , CM000669.2:g.96184087del	GRCh38
NC_000007.13:g.95813399del , CM000669.1:g.95813399del	GRCh37
NC_000007.12:g.95651335del	NCBI36
NG_012247.1:g.143064del
NG_012247.2:g.143064del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1177+193del MANE Select	ENSP00000265631.6:n.1177+193del
ENST00000265631.9:c.1177+193del	ENSP00000265631.5:n.1177+193del
ENST00000416240.6:c.1180+193del	ENSP00000400101.2:n.1180+193del
ENST00000484495.5:n.330+193del
ENST00000490072.5:n.244+193del
ENST00000492869.1:n.298+193del
NM_001160210.1:c.1180+193del	NP_001153682.1:n.1180+193del
NM_014251.2:c.1177+193del	NP_055066.1:n.1177+193del
NR_027662.1:n.1252+193del
XM_006715831.2:c.1210+193del	XP_006715894.1:n.1210+193del
XM_011515727.1:c.1210+193del	XP_011514029.1:n.1210+193del
XM_011515728.1:c.325+193del	XP_011514030.1:n.325+193del
XM_006715831.4:c.1210+193del	XP_006715894.1:n.1210+193del
XM_011515727.3:c.1210+193del	XP_011514029.1:n.1210+193del
XM_017011663.1:c.1168+193del	XP_016867152.1:n.1168+193del
XM_017011664.2:c.325+193del	XP_016867153.1:n.325+193del
XM_017011665.1:c.325+193del	XP_016867154.1:n.325+193del
XR_001744525.2:n.1348+193del
XR_002956405.1:n.1981+193del
NM_014251.3:c.1177+193del MANE Select	NP_055066.1:n.1177+193del
NR_027662.2:n.1203+193del
NM_001160210.2:c.1180+193del	NP_001153682.1:n.1180+193del