Canonical Allele Identifier: CA2683824595
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96121610_96121615del , CM000669.2:g.96121610_96121615del GRCh38
NC_000007.13:g.95750922_95750927del , CM000669.1:g.95750922_95750927del GRCh37
NC_000007.12:g.95588858_95588863del NCBI36
NG_012247.1:g.205537_205542del
NG_012247.2:g.205537_205542del

Transcript Alleles

HGVS Amino-acid change
ENST00000265631.10:c.1841+44_1841+49del MANE Select ENSP00000265631.6:n.1841+44_1841+49del
ENST00000265631.9:c.1841+44_1841+49del ENSP00000265631.5:n.1841+44_1841+49del
ENST00000416240.6:c.1844+44_1844+49del ENSP00000400101.2:n.1844+44_1844+49del
ENST00000494085.1:n.344+44_344+49del
NM_001160210.1:c.1844+44_1844+49del NP_001153682.1:n.1844+44_1844+49del
NM_014251.2:c.1841+44_1841+49del NP_055066.1:n.1841+44_1841+49del
NR_027662.1:n.1916+44_1916+49del
XM_006715831.2:c.1874+44_1874+49del XP_006715894.1:n.1874+44_1874+49del
XM_011515728.1:c.989+44_989+49del XP_011514030.1:n.989+44_989+49del
XM_006715831.4:c.1874+44_1874+49del XP_006715894.1:n.1874+44_1874+49del
XM_017011663.1:c.1832+44_1832+49del XP_016867152.1:n.1832+44_1832+49del
XM_017011664.2:c.989+44_989+49del XP_016867153.1:n.989+44_989+49del
XM_017011665.1:c.989+44_989+49del XP_016867154.1:n.989+44_989+49del
XR_001744525.2:n.2087+44_2087+49del
XR_002956405.1:n.2645+44_2645+49del
NM_014251.3:c.1841+44_1841+49del MANE Select NP_055066.1:n.1841+44_1841+49del
NR_027662.2:n.1867+44_1867+49del
NM_001160210.2:c.1844+44_1844+49del NP_001153682.1:n.1844+44_1844+49del