Canonical Allele Identifier: CA2683825544

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96189552-CAAAAAAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189563_96189570del , CM000669.2:g.96189563_96189570del	GRCh38
NC_000007.13:g.95818875_95818882del , CM000669.1:g.95818875_95818882del	GRCh37
NC_000007.12:g.95656811_95656818del	NCBI36
NG_012247.1:g.137588_137595del
NG_012247.2:g.137588_137595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+21_848+28del MANE Select	ENSP00000265631.6:n.848+21_848+28del
ENST00000265631.9:c.848+21_848+28del	ENSP00000265631.5:n.848+21_848+28del
ENST00000416240.6:c.848+21_848+28del	ENSP00000400101.2:n.848+21_848+28del
NM_001160210.1:c.848+21_848+28del	NP_001153682.1:n.848+21_848+28del
NM_014251.2:c.848+21_848+28del	NP_055066.1:n.848+21_848+28del
NR_027662.1:n.923+21_923+28del
XM_006715831.2:c.881+21_881+28del	XP_006715894.1:n.881+21_881+28del
XM_011515727.1:c.881+21_881+28del	XP_011514029.1:n.881+21_881+28del
XM_011515728.1:c.-4-182_-4-175del	XP_011514030.1:n.-4-182_-4-175del
XM_006715831.4:c.881+21_881+28del	XP_006715894.1:n.881+21_881+28del
XM_011515727.3:c.881+21_881+28del	XP_011514029.1:n.881+21_881+28del
XM_017011663.1:c.839+21_839+28del	XP_016867152.1:n.839+21_839+28del
XM_017011664.2:c.-4-182_-4-175del	XP_016867153.1:n.-4-182_-4-175del
XM_017011665.1:c.-4-182_-4-175del	XP_016867154.1:n.-4-182_-4-175del
XR_001744525.2:n.1019+21_1019+28del
XR_002956405.1:n.1161+21_1161+28del
NM_014251.3:c.848+21_848+28del MANE Select	NP_055066.1:n.848+21_848+28del
NR_027662.2:n.874+21_874+28del
NM_001160210.2:c.848+21_848+28del	NP_001153682.1:n.848+21_848+28del