Canonical Allele Identifier: CA1727580545
Gene: SLC25A13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189548_96189549delinsAT , CM000669.2:g.96189548_96189549delinsAT GRCh38
NC_000007.13:g.95818860_95818861delinsAT , CM000669.1:g.95818860_95818861delinsAT GRCh37
NC_000007.12:g.95656796_95656797delinsAT NCBI36
NG_012247.1:g.137599_137600delinsAT
NG_012247.2:g.137599_137600delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.848+32_848+33delinsAT MANE Select ENSP00000265631.6:n.848+32_848+33delinsAT
ENST00000265631.9:c.848+32_848+33delinsAT ENSP00000265631.5:n.848+32_848+33delinsAT
ENST00000416240.6:c.848+32_848+33delinsAT ENSP00000400101.2:n.848+32_848+33delinsAT
NM_001160210.1:c.848+32_848+33delinsAT NP_001153682.1:n.848+32_848+33delinsAT
NM_014251.2:c.848+32_848+33delinsAT NP_055066.1:n.848+32_848+33delinsAT
NR_027662.1:n.923+32_923+33delinsAT
XM_006715831.2:c.881+32_881+33delinsAT XP_006715894.1:n.881+32_881+33delinsAT
XM_011515727.1:c.881+32_881+33delinsAT XP_011514029.1:n.881+32_881+33delinsAT
XM_011515728.1:c.-4-171_-4-170delinsAT XP_011514030.1:n.-4-171_-4-170delinsAT
XM_006715831.4:c.881+32_881+33delinsAT XP_006715894.1:n.881+32_881+33delinsAT
XM_011515727.3:c.881+32_881+33delinsAT XP_011514029.1:n.881+32_881+33delinsAT
XM_017011663.1:c.839+32_839+33delinsAT XP_016867152.1:n.839+32_839+33delinsAT
XM_017011664.2:c.-4-171_-4-170delinsAT XP_016867153.1:n.-4-171_-4-170delinsAT
XM_017011665.1:c.-4-171_-4-170delinsAT XP_016867154.1:n.-4-171_-4-170delinsAT
XR_001744525.2:n.1019+32_1019+33delinsAT
XR_002956405.1:n.1161+32_1161+33delinsAT
NM_014251.3:c.848+32_848+33delinsAT MANE Select NP_055066.1:n.848+32_848+33delinsAT
NR_027662.2:n.874+32_874+33delinsAT
NM_001160210.2:c.848+32_848+33delinsAT NP_001153682.1:n.848+32_848+33delinsAT