Canonical Allele Identifier: CA2578945818

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121327del , CM000669.2:g.96121327del	GRCh38
NC_000007.13:g.95750639del , CM000669.1:g.95750639del	GRCh37
NC_000007.12:g.95588575del	NCBI36
NG_012247.1:g.205824del
NG_012247.2:g.205824del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1895del MANE Select	ENSP00000265631.6:p.Pro632ArgfsTer?
ENST00000265631.9:c.1895del	ENSP00000265631.5:p.Pro632ArgfsTer?
ENST00000416240.6:c.1898del	ENSP00000400101.2:p.Pro633ArgfsTer?
ENST00000494085.1:n.398del
NM_001160210.1:c.1898del	NP_001153682.1:p.Pro633ArgfsTer?
NM_014251.2:c.1895del	NP_055066.1:p.Pro632ArgfsTer?
NR_027662.1:n.1970del
XM_006715831.2:c.1928del	XP_006715894.1:p.Pro643ArgfsTer?
XM_011515728.1:c.1043del	XP_011514030.1:p.Pro348ArgfsTer?
XM_006715831.4:c.1928del	XP_006715894.1:p.Pro643ArgfsTer?
XM_017011663.1:c.1886del	XP_016867152.1:p.Pro629ArgfsTer?
XM_017011664.2:c.1043del	XP_016867153.1:p.Pro348ArgfsTer?
XM_017011665.1:c.1043del	XP_016867154.1:p.Pro348ArgfsTer?
XR_001744525.2:n.2141del
XR_002956405.1:n.2699del
NM_014251.3:c.1895del MANE Select	NP_055066.1:p.Pro632ArgfsTer?
NR_027662.2:n.1921del
NM_001160210.2:c.1898del	NP_001153682.1:p.Pro633ArgfsTer?