Canonical Allele Identifier: CA576707780

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1163960544
• gnomAD v2: 7-95750725-TTTTG-T
• gnomAD v3: 7-96121413-TTTTG-T
• gnomAD v4: 7-96121413-TTTTG-T
• MyVariant Identifiers: chr7:g.95750726_95750729del (hg19) ; chr7:g.96121414_96121417del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121421_96121424del , CM000669.2:g.96121421_96121424del	GRCh38
NC_000007.13:g.95750733_95750736del , CM000669.1:g.95750733_95750736del	GRCh37
NC_000007.12:g.95588669_95588672del	NCBI36
NG_012247.1:g.205731_205734del
NG_012247.2:g.205731_205734del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1842-40_1842-37del MANE Select	ENSP00000265631.6:n.1842-40_1842-37del
ENST00000265631.9:c.1842-40_1842-37del	ENSP00000265631.5:n.1842-40_1842-37del
ENST00000416240.6:c.1845-40_1845-37del	ENSP00000400101.2:n.1845-40_1845-37del
ENST00000494085.1:n.345-40_345-37del
NM_001160210.1:c.1845-40_1845-37del	NP_001153682.1:n.1845-40_1845-37del
NM_014251.2:c.1842-40_1842-37del	NP_055066.1:n.1842-40_1842-37del
NR_027662.1:n.1917-40_1917-37del
XM_006715831.2:c.1875-40_1875-37del	XP_006715894.1:n.1875-40_1875-37del
XM_011515728.1:c.990-40_990-37del	XP_011514030.1:n.990-40_990-37del
XM_006715831.4:c.1875-40_1875-37del	XP_006715894.1:n.1875-40_1875-37del
XM_017011663.1:c.1833-40_1833-37del	XP_016867152.1:n.1833-40_1833-37del
XM_017011664.2:c.990-40_990-37del	XP_016867153.1:n.990-40_990-37del
XM_017011665.1:c.990-40_990-37del	XP_016867154.1:n.990-40_990-37del
XR_001744525.2:n.2088-40_2088-37del
XR_002956405.1:n.2646-40_2646-37del
NM_014251.3:c.1842-40_1842-37del MANE Select	NP_055066.1:n.1842-40_1842-37del
NR_027662.2:n.1868-40_1868-37del
NM_001160210.2:c.1845-40_1845-37del	NP_001153682.1:n.1845-40_1845-37del