Canonical Allele Identifier: CA456632271

Gene: SLC25A13

Linked Data

• COSMIC: COSM453615
• MyVariant Identifiers: chr7:g.95751180del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121869del , CM000669.2:g.96121869del	GRCh38
NC_000007.13:g.95751181del , CM000669.1:g.95751181del	GRCh37
NC_000007.12:g.95589117del	NCBI36
NG_012247.1:g.205280del
NG_012247.2:g.205280del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1721del MANE Select	ENSP00000265631.6:p.Gly574AspfsTer22
ENST00000265631.9:c.1721del	ENSP00000265631.5:p.Gly574AspfsTer22
ENST00000416240.6:c.1724del	ENSP00000400101.2:p.Gly575AspfsTer22
ENST00000494085.1:n.131del
NM_001160210.1:c.1724del	NP_001153682.1:p.Gly575AspfsTer22
NM_014251.2:c.1721del	NP_055066.1:p.Gly574AspfsTer22
NR_027662.1:n.1796del
XM_006715831.2:c.1754del	XP_006715894.1:p.Gly585AspfsTer22
XM_011515728.1:c.869del	XP_011514030.1:p.Gly290AspfsTer22
XM_006715831.4:c.1754del	XP_006715894.1:p.Gly585AspfsTer22
XM_017011663.1:c.1712del	XP_016867152.1:p.Gly571AspfsTer22
XM_017011664.2:c.869del	XP_016867153.1:p.Gly290AspfsTer22
XM_017011665.1:c.869del	XP_016867154.1:p.Gly290AspfsTer22
XR_001744525.2:n.1967del
XR_002956405.1:n.2525del
NM_014251.3:c.1721del MANE Select	NP_055066.1:p.Gly574AspfsTer22
NR_027662.2:n.1747del
NM_001160210.2:c.1724del	NP_001153682.1:p.Gly575AspfsTer22