Canonical Allele Identifier: CA2683825474

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96189487-T-TCAGTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189488_96189494dup , CM000669.2:g.96189488_96189494dup	GRCh38
NC_000007.13:g.95818800_95818806dup , CM000669.1:g.95818800_95818806dup	GRCh37
NC_000007.12:g.95656736_95656742dup	NCBI36
NG_012247.1:g.137654_137660dup
NG_012247.2:g.137654_137660dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+87_848+93dup MANE Select	ENSP00000265631.6:n.848+87_848+93dup
ENST00000265631.9:c.848+87_848+93dup	ENSP00000265631.5:n.848+87_848+93dup
ENST00000416240.6:c.848+87_848+93dup	ENSP00000400101.2:n.848+87_848+93dup
NM_001160210.1:c.848+87_848+93dup	NP_001153682.1:n.848+87_848+93dup
NM_014251.2:c.848+87_848+93dup	NP_055066.1:n.848+87_848+93dup
NR_027662.1:n.923+87_923+93dup
XM_006715831.2:c.881+87_881+93dup	XP_006715894.1:n.881+87_881+93dup
XM_011515727.1:c.881+87_881+93dup	XP_011514029.1:n.881+87_881+93dup
XM_011515728.1:c.-4-116_-4-110dup	XP_011514030.1:n.-4-116_-4-110dup
XM_006715831.4:c.881+87_881+93dup	XP_006715894.1:n.881+87_881+93dup
XM_011515727.3:c.881+87_881+93dup	XP_011514029.1:n.881+87_881+93dup
XM_017011663.1:c.839+87_839+93dup	XP_016867152.1:n.839+87_839+93dup
XM_017011664.2:c.-4-116_-4-110dup	XP_016867153.1:n.-4-116_-4-110dup
XM_017011665.1:c.-4-116_-4-110dup	XP_016867154.1:n.-4-116_-4-110dup
XR_001744525.2:n.1019+87_1019+93dup
XR_002956405.1:n.1161+87_1161+93dup
NM_014251.3:c.848+87_848+93dup MANE Select	NP_055066.1:n.848+87_848+93dup
NR_027662.2:n.874+87_874+93dup
NM_001160210.2:c.848+87_848+93dup	NP_001153682.1:n.848+87_848+93dup