Canonical Allele Identifier: CA891862725
Gene: SLC25A13 HGNC NCBI

Linked Data

dbSNP Id: rs1562774655

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96121926_96121927insCCGGGCAGCCACCTGTAATCTCC , CM000669.2:g.96121926_96121927insCCGGGCAGCCACCTGTAATCTCC GRCh38
NC_000007.13:g.95751238_95751239insCCGGGCAGCCACCTGTAATCTCC , CM000669.1:g.95751238_95751239insCCGGGCAGCCACCTGTAATCTCC GRCh37
NC_000007.12:g.95589174_95589175insCCGGGCAGCCACCTGTAATCTCC NCBI36
NG_012247.1:g.205223_205224insAGATTACAGGTGGCTGCCCGGGG
NG_012247.2:g.205223_205224insAGATTACAGGTGGCTGCCCGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.1664_1665insAGATTACAGGTGGCTGCCCGGGG MANE Select ENSP00000265631.6:p.Gln556AspfsTer15
ENST00000265631.9:c.1664_1665insAGATTACAGGTGGCTGCCCGGGG ENSP00000265631.5:p.Gln556AspfsTer15
ENST00000416240.6:c.1667_1668insAGATTACAGGTGGCTGCCCGGGG ENSP00000400101.2:p.Gln557AspfsTer15
ENST00000494085.1:n.74_75insAGATTACAGGTGGCTGCCCGGGG
NM_001160210.1:c.1667_1668insAGATTACAGGTGGCTGCCCGGGG NP_001153682.1:p.Gln557AspfsTer15
NM_014251.2:c.1664_1665insAGATTACAGGTGGCTGCCCGGGG NP_055066.1:p.Gln556AspfsTer15
NR_027662.1:n.1739_1740insAGATTACAGGTGGCTGCCCGGGG
XM_006715831.2:c.1697_1698insAGATTACAGGTGGCTGCCCGGGG XP_006715894.1:p.Gln567AspfsTer15
XM_011515728.1:c.812_813insAGATTACAGGTGGCTGCCCGGGG XP_011514030.1:p.Gln272AspfsTer15
XM_006715831.4:c.1697_1698insAGATTACAGGTGGCTGCCCGGGG XP_006715894.1:p.Gln567AspfsTer15
XM_017011663.1:c.1655_1656insAGATTACAGGTGGCTGCCCGGGG XP_016867152.1:p.Gln553AspfsTer15
XM_017011664.2:c.812_813insAGATTACAGGTGGCTGCCCGGGG XP_016867153.1:p.Gln272AspfsTer15
XM_017011665.1:c.812_813insAGATTACAGGTGGCTGCCCGGGG XP_016867154.1:p.Gln272AspfsTer15
XR_001744525.2:n.1910_1911insAGATTACAGGTGGCTGCCCGGGG
XR_002956405.1:n.2468_2469insAGATTACAGGTGGCTGCCCGGGG
NM_014251.3:c.1664_1665insAGATTACAGGTGGCTGCCCGGGG MANE Select NP_055066.1:p.Gln556AspfsTer15
NR_027662.2:n.1690_1691insAGATTACAGGTGGCTGCCCGGGG
NM_001160210.2:c.1667_1668insAGATTACAGGTGGCTGCCCGGGG NP_001153682.1:p.Gln557AspfsTer15