Canonical Allele Identifier: CA2683825501
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189522_96189527del , CM000669.2:g.96189522_96189527del GRCh38
NC_000007.13:g.95818834_95818839del , CM000669.1:g.95818834_95818839del GRCh37
NC_000007.12:g.95656770_95656775del NCBI36
NG_012247.1:g.137624_137629del
NG_012247.2:g.137624_137629del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.848+57_848+62del MANE Select ENSP00000265631.6:n.848+57_848+62del
ENST00000265631.9:c.848+57_848+62del ENSP00000265631.5:n.848+57_848+62del
ENST00000416240.6:c.848+57_848+62del ENSP00000400101.2:n.848+57_848+62del
NM_001160210.1:c.848+57_848+62del NP_001153682.1:n.848+57_848+62del
NM_014251.2:c.848+57_848+62del NP_055066.1:n.848+57_848+62del
NR_027662.1:n.923+57_923+62del
XM_006715831.2:c.881+57_881+62del XP_006715894.1:n.881+57_881+62del
XM_011515727.1:c.881+57_881+62del XP_011514029.1:n.881+57_881+62del
XM_011515728.1:c.-4-146_-4-141del XP_011514030.1:n.-4-146_-4-141del
XM_006715831.4:c.881+57_881+62del XP_006715894.1:n.881+57_881+62del
XM_011515727.3:c.881+57_881+62del XP_011514029.1:n.881+57_881+62del
XM_017011663.1:c.839+57_839+62del XP_016867152.1:n.839+57_839+62del
XM_017011664.2:c.-4-146_-4-141del XP_016867153.1:n.-4-146_-4-141del
XM_017011665.1:c.-4-146_-4-141del XP_016867154.1:n.-4-146_-4-141del
XR_001744525.2:n.1019+57_1019+62del
XR_002956405.1:n.1161+57_1161+62del
NM_014251.3:c.848+57_848+62del MANE Select NP_055066.1:n.848+57_848+62del
NR_027662.2:n.874+57_874+62del
NM_001160210.2:c.848+57_848+62del NP_001153682.1:n.848+57_848+62del