Canonical Allele Identifier: CA2777032062

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189550_96189551del , CM000669.2:g.96189550_96189551del	GRCh38
NC_000007.13:g.95818862_95818863del , CM000669.1:g.95818862_95818863del	GRCh37
NC_000007.12:g.95656798_95656799del	NCBI36
NG_012247.1:g.137597_137598del
NG_012247.2:g.137597_137598del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+30_848+31del MANE Select	ENSP00000265631.6:n.848+30_848+31del
ENST00000265631.9:c.848+30_848+31del	ENSP00000265631.5:n.848+30_848+31del
ENST00000416240.6:c.848+30_848+31del	ENSP00000400101.2:n.848+30_848+31del
NM_001160210.1:c.848+30_848+31del	NP_001153682.1:n.848+30_848+31del
NM_014251.2:c.848+30_848+31del	NP_055066.1:n.848+30_848+31del
NR_027662.1:n.923+30_923+31del
XM_006715831.2:c.881+30_881+31del	XP_006715894.1:n.881+30_881+31del
XM_011515727.1:c.881+30_881+31del	XP_011514029.1:n.881+30_881+31del
XM_011515728.1:c.-4-173_-4-172del	XP_011514030.1:n.-4-173_-4-172del
XM_006715831.4:c.881+30_881+31del	XP_006715894.1:n.881+30_881+31del
XM_011515727.3:c.881+30_881+31del	XP_011514029.1:n.881+30_881+31del
XM_017011663.1:c.839+30_839+31del	XP_016867152.1:n.839+30_839+31del
XM_017011664.2:c.-4-173_-4-172del	XP_016867153.1:n.-4-173_-4-172del
XM_017011665.1:c.-4-173_-4-172del	XP_016867154.1:n.-4-173_-4-172del
XR_001744525.2:n.1019+30_1019+31del
XR_002956405.1:n.1161+30_1161+31del
NM_014251.3:c.848+30_848+31del MANE Select	NP_055066.1:n.848+30_848+31del
NR_027662.2:n.874+30_874+31del
NM_001160210.2:c.848+30_848+31del	NP_001153682.1:n.848+30_848+31del