Canonical Allele Identifier: CA1727518163

Gene: SLC25A13

Linked Data

• dbSNP Id: rs1791521197
• gnomAD v4: 7-96121805-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121807_96121808del , CM000669.2:g.96121807_96121808del	GRCh38
NC_000007.13:g.95751119_95751120del , CM000669.1:g.95751119_95751120del	GRCh37
NC_000007.12:g.95589055_95589056del	NCBI36
NG_012247.1:g.205341_205342del
NG_012247.2:g.205341_205342del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1750+32_1750+33del MANE Select	ENSP00000265631.6:n.1750+32_1750+33del
ENST00000265631.9:c.1750+32_1750+33del	ENSP00000265631.5:n.1750+32_1750+33del
ENST00000416240.6:c.1753+32_1753+33del	ENSP00000400101.2:n.1753+32_1753+33del
ENST00000494085.1:n.192_193del
NM_001160210.1:c.1753+32_1753+33del	NP_001153682.1:n.1753+32_1753+33del
NM_014251.2:c.1750+32_1750+33del	NP_055066.1:n.1750+32_1750+33del
NR_027662.1:n.1825+32_1825+33del
XM_006715831.2:c.1783+32_1783+33del	XP_006715894.1:n.1783+32_1783+33del
XM_011515728.1:c.898+32_898+33del	XP_011514030.1:n.898+32_898+33del
XM_006715831.4:c.1783+32_1783+33del	XP_006715894.1:n.1783+32_1783+33del
XM_017011663.1:c.1741+32_1741+33del	XP_016867152.1:n.1741+32_1741+33del
XM_017011664.2:c.898+32_898+33del	XP_016867153.1:n.898+32_898+33del
XM_017011665.1:c.898+32_898+33del	XP_016867154.1:n.898+32_898+33del
XR_001744525.2:n.1996+32_1996+33del
XR_002956405.1:n.2554+32_2554+33del
NM_014251.3:c.1750+32_1750+33del MANE Select	NP_055066.1:n.1750+32_1750+33del
NR_027662.2:n.1776+32_1776+33del
NM_001160210.2:c.1753+32_1753+33del	NP_001153682.1:n.1753+32_1753+33del