Canonical Allele Identifier: CA2683825546
Gene: SLC25A13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.96189566_96189570dup , CM000669.2:g.96189566_96189570dup GRCh38
NC_000007.13:g.95818878_95818882dup , CM000669.1:g.95818878_95818882dup GRCh37
NC_000007.12:g.95656814_95656818dup NCBI36
NG_012247.1:g.137591_137595dup
NG_012247.2:g.137591_137595dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000265631.10:c.848+24_848+28dup MANE Select ENSP00000265631.6:n.848+24_848+28dup
ENST00000265631.9:c.848+24_848+28dup ENSP00000265631.5:n.848+24_848+28dup
ENST00000416240.6:c.848+24_848+28dup ENSP00000400101.2:n.848+24_848+28dup
NM_001160210.1:c.848+24_848+28dup NP_001153682.1:n.848+24_848+28dup
NM_014251.2:c.848+24_848+28dup NP_055066.1:n.848+24_848+28dup
NR_027662.1:n.923+24_923+28dup
XM_006715831.2:c.881+24_881+28dup XP_006715894.1:n.881+24_881+28dup
XM_011515727.1:c.881+24_881+28dup XP_011514029.1:n.881+24_881+28dup
XM_011515728.1:c.-4-179_-4-175dup XP_011514030.1:n.-4-179_-4-175dup
XM_006715831.4:c.881+24_881+28dup XP_006715894.1:n.881+24_881+28dup
XM_011515727.3:c.881+24_881+28dup XP_011514029.1:n.881+24_881+28dup
XM_017011663.1:c.839+24_839+28dup XP_016867152.1:n.839+24_839+28dup
XM_017011664.2:c.-4-179_-4-175dup XP_016867153.1:n.-4-179_-4-175dup
XM_017011665.1:c.-4-179_-4-175dup XP_016867154.1:n.-4-179_-4-175dup
XR_001744525.2:n.1019+24_1019+28dup
XR_002956405.1:n.1161+24_1161+28dup
NM_014251.3:c.848+24_848+28dup MANE Select NP_055066.1:n.848+24_848+28dup
NR_027662.2:n.874+24_874+28dup
NM_001160210.2:c.848+24_848+28dup NP_001153682.1:n.848+24_848+28dup