Canonical Allele Identifier: CA1727518159

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121805_96121807delinsCAA , CM000669.2:g.96121805_96121807delinsCAA	GRCh38
NC_000007.13:g.95751117_95751119delinsCAA , CM000669.1:g.95751117_95751119delinsCAA	GRCh37
NC_000007.12:g.95589053_95589055delinsCAA	NCBI36
NG_012247.1:g.205341_205343delinsTTG
NG_012247.2:g.205341_205343delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1750+32_1750+34delinsTTG MANE Select	ENSP00000265631.6:n.1750+32_1750+34delinsTTG
ENST00000265631.9:c.1750+32_1750+34delinsTTG	ENSP00000265631.5:n.1750+32_1750+34delinsTTG
ENST00000416240.6:c.1753+32_1753+34delinsTTG	ENSP00000400101.2:n.1753+32_1753+34delinsTTG
ENST00000494085.1:n.192_194delinsTTG
NM_001160210.1:c.1753+32_1753+34delinsTTG	NP_001153682.1:n.1753+32_1753+34delinsTTG
NM_014251.2:c.1750+32_1750+34delinsTTG	NP_055066.1:n.1750+32_1750+34delinsTTG
NR_027662.1:n.1825+32_1825+34delinsTTG
XM_006715831.2:c.1783+32_1783+34delinsTTG	XP_006715894.1:n.1783+32_1783+34delinsTTG
XM_011515728.1:c.898+32_898+34delinsTTG	XP_011514030.1:n.898+32_898+34delinsTTG
XM_006715831.4:c.1783+32_1783+34delinsTTG	XP_006715894.1:n.1783+32_1783+34delinsTTG
XM_017011663.1:c.1741+32_1741+34delinsTTG	XP_016867152.1:n.1741+32_1741+34delinsTTG
XM_017011664.2:c.898+32_898+34delinsTTG	XP_016867153.1:n.898+32_898+34delinsTTG
XM_017011665.1:c.898+32_898+34delinsTTG	XP_016867154.1:n.898+32_898+34delinsTTG
XR_001744525.2:n.1996+32_1996+34delinsTTG
XR_002956405.1:n.2554+32_2554+34delinsTTG
NM_014251.3:c.1750+32_1750+34delinsTTG MANE Select	NP_055066.1:n.1750+32_1750+34delinsTTG
NR_027662.2:n.1776+32_1776+34delinsTTG
NM_001160210.2:c.1753+32_1753+34delinsTTG	NP_001153682.1:n.1753+32_1753+34delinsTTG