Canonical Allele Identifier: CA2715169157

Gene: SLC25A13

Linked Data

• dbSNP Id: rs2116381351

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121419_96121420insAACATCAGCAGGGGTCACTAAAGA , CM000669.2:g.96121419_96121420insAACATCAGCAGGGGTCACTAAAGA	GRCh38
NC_000007.13:g.95750731_95750732insAACATCAGCAGGGGTCACTAAAGA , CM000669.1:g.95750731_95750732insAACATCAGCAGGGGTCACTAAAGA	GRCh37
NC_000007.12:g.95588667_95588668insAACATCAGCAGGGGTCACTAAAGA	NCBI36
NG_012247.1:g.205728_205729insTCTTTAGTGACCCCTGCTGATGTT
NG_012247.2:g.205728_205729insTCTTTAGTGACCCCTGCTGATGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1842-43_1842-42insTCTTTAGTGACCCCTGCTGATGTT MANE Select	ENSP00000265631.6:n.1842-43_1842-42insTCTTTAGTGACCCCTGCTGATGT...
ENST00000265631.9:c.1842-43_1842-42insTCTTTAGTGACCCCTGCTGATGTT	ENSP00000265631.5:n.1842-43_1842-42insTCTTTAGTGACCCCTGCTGATGT...
ENST00000416240.6:c.1845-43_1845-42insTCTTTAGTGACCCCTGCTGATGTT	ENSP00000400101.2:n.1845-43_1845-42insTCTTTAGTGACCCCTGCTGATGT...
ENST00000494085.1:n.345-43_345-42insTCTTTAGTGACCCCTGCTGATGTT
NM_001160210.1:c.1845-43_1845-42insTCTTTAGTGACCCCTGCTGATGTT	NP_001153682.1:n.1845-43_1845-42insTCTTTAGTGACCCCTGCTGATGTT
NM_014251.2:c.1842-43_1842-42insTCTTTAGTGACCCCTGCTGATGTT	NP_055066.1:n.1842-43_1842-42insTCTTTAGTGACCCCTGCTGATGTT
NR_027662.1:n.1917-43_1917-42insTCTTTAGTGACCCCTGCTGATGTT
XM_006715831.2:c.1875-43_1875-42insTCTTTAGTGACCCCTGCTGATGTT	XP_006715894.1:n.1875-43_1875-42insTCTTTAGTGACCCCTGCTGATGTT
XM_011515728.1:c.990-43_990-42insTCTTTAGTGACCCCTGCTGATGTT	XP_011514030.1:n.990-43_990-42insTCTTTAGTGACCCCTGCTGATGTT
XM_006715831.4:c.1875-43_1875-42insTCTTTAGTGACCCCTGCTGATGTT	XP_006715894.1:n.1875-43_1875-42insTCTTTAGTGACCCCTGCTGATGTT
XM_017011663.1:c.1833-43_1833-42insTCTTTAGTGACCCCTGCTGATGTT	XP_016867152.1:n.1833-43_1833-42insTCTTTAGTGACCCCTGCTGATGTT
XM_017011664.2:c.990-43_990-42insTCTTTAGTGACCCCTGCTGATGTT	XP_016867153.1:n.990-43_990-42insTCTTTAGTGACCCCTGCTGATGTT
XM_017011665.1:c.990-43_990-42insTCTTTAGTGACCCCTGCTGATGTT	XP_016867154.1:n.990-43_990-42insTCTTTAGTGACCCCTGCTGATGTT
XR_001744525.2:n.2088-43_2088-42insTCTTTAGTGACCCCTGCTGATGTT
XR_002956405.1:n.2646-43_2646-42insTCTTTAGTGACCCCTGCTGATGTT
NM_014251.3:c.1842-43_1842-42insTCTTTAGTGACCCCTGCTGATGTT MANE Select	NP_055066.1:n.1842-43_1842-42insTCTTTAGTGACCCCTGCTGATGTT
NR_027662.2:n.1868-43_1868-42insTCTTTAGTGACCCCTGCTGATGTT
NM_001160210.2:c.1845-43_1845-42insTCTTTAGTGACCCCTGCTGATGTT	NP_001153682.1:n.1845-43_1845-42insTCTTTAGTGACCCCTGCTGATGTT