Canonical Allele Identifier: CA918078444

Gene: SLC25A13

Linked Data

• dbSNP Id: rs11335226
• gnomAD v3: 7-96189552-C-CAAAAAA
• gnomAD v4: 7-96189552-C-CAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189565_96189570dup , CM000669.2:g.96189565_96189570dup	GRCh38
NC_000007.13:g.95818877_95818882dup , CM000669.1:g.95818877_95818882dup	GRCh37
NC_000007.12:g.95656813_95656818dup	NCBI36
NG_012247.1:g.137590_137595dup
NG_012247.2:g.137590_137595dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+23_848+28dup MANE Select	ENSP00000265631.6:n.848+23_848+28dup
ENST00000265631.9:c.848+23_848+28dup	ENSP00000265631.5:n.848+23_848+28dup
ENST00000416240.6:c.848+23_848+28dup	ENSP00000400101.2:n.848+23_848+28dup
NM_001160210.1:c.848+23_848+28dup	NP_001153682.1:n.848+23_848+28dup
NM_014251.2:c.848+23_848+28dup	NP_055066.1:n.848+23_848+28dup
NR_027662.1:n.923+23_923+28dup
XM_006715831.2:c.881+23_881+28dup	XP_006715894.1:n.881+23_881+28dup
XM_011515727.1:c.881+23_881+28dup	XP_011514029.1:n.881+23_881+28dup
XM_011515728.1:c.-4-180_-4-175dup	XP_011514030.1:n.-4-180_-4-175dup
XM_006715831.4:c.881+23_881+28dup	XP_006715894.1:n.881+23_881+28dup
XM_011515727.3:c.881+23_881+28dup	XP_011514029.1:n.881+23_881+28dup
XM_017011663.1:c.839+23_839+28dup	XP_016867152.1:n.839+23_839+28dup
XM_017011664.2:c.-4-180_-4-175dup	XP_016867153.1:n.-4-180_-4-175dup
XM_017011665.1:c.-4-180_-4-175dup	XP_016867154.1:n.-4-180_-4-175dup
XR_001744525.2:n.1019+23_1019+28dup
XR_002956405.1:n.1161+23_1161+28dup
NM_014251.3:c.848+23_848+28dup MANE Select	NP_055066.1:n.848+23_848+28dup
NR_027662.2:n.874+23_874+28dup
NM_001160210.2:c.848+23_848+28dup	NP_001153682.1:n.848+23_848+28dup