Canonical Allele Identifier: CA2683824397

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96121278-AAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121279_96121281del , CM000669.2:g.96121279_96121281del	GRCh38
NC_000007.13:g.95750591_95750593del , CM000669.1:g.95750591_95750593del	GRCh37
NC_000007.12:g.95588527_95588529del	NCBI36
NG_012247.1:g.205867_205869del
NG_012247.2:g.205867_205869del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1938_1940del MANE Select	ENSP00000265631.6:p.Phe647del
ENST00000265631.9:c.1938_1940del	ENSP00000265631.5:p.Phe647del
ENST00000416240.6:c.1941_1943del	ENSP00000400101.2:p.Phe648del
ENST00000494085.1:n.441_443del
NM_001160210.1:c.1941_1943del	NP_001153682.1:p.Phe648del
NM_014251.2:c.1938_1940del	NP_055066.1:p.Phe647del
NR_027662.1:n.2013_2015del
XM_006715831.2:c.1971_1973del	XP_006715894.1:p.Phe658del
XM_011515728.1:c.1086_1088del	XP_011514030.1:p.Phe363del
XM_006715831.4:c.1971_1973del	XP_006715894.1:p.Phe658del
XM_017011663.1:c.1929_1931del	XP_016867152.1:p.Phe644del
XM_017011664.2:c.1086_1088del	XP_016867153.1:p.Phe363del
XM_017011665.1:c.1086_1088del	XP_016867154.1:p.Phe363del
XR_001744525.2:n.2184_2186del
XR_002956405.1:n.2742_2744del
NM_014251.3:c.1938_1940del MANE Select	NP_055066.1:p.Phe647del
NR_027662.2:n.1964_1966del
NM_001160210.2:c.1941_1943del	NP_001153682.1:p.Phe648del