Canonical Allele Identifier: CA2246233512

Gene: RANGRF SLC25A35

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288981_8288984delinsCAAG , CM000679.2:g.8288981_8288984delinsCAAG	GRCh38
NC_000017.10:g.8192299_8192302delinsCAAG , CM000679.1:g.8192299_8192302delinsCAAG	GRCh37
NC_000017.9:g.8133024_8133027delinsCAAG	NCBI36
NG_028189.1:g.5331_5334delinsCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.103_106delinsCAAG (RANGRF) MANE Select	ENSP00000226105.6:p.Gln35=
ENST00000226105.10:c.103_106delinsCAAG (RANGRF)	ENSP00000226105.6:p.Gln35=
ENST00000380067.6:c.*632_*635delinsCTTG (SLC25A35)	ENSP00000369407.2:n.*632_*635delinsCTTG
ENST00000407006.8:c.103_106delinsCAAG (RANGRF)	ENSP00000383940.4:p.Gln35=
ENST00000439238.3:c.103_106delinsCAAG (RANGRF)	ENSP00000413190.3:p.Gln35=
ENST00000578849.1:n.193_196delinsCAAG (RANGRF)
ENST00000579192.5:c.*43-552_*43-549delinsCTTG (SLC25A35)	ENSP00000462395.1:n.*43-552_*43-549delinsCTTG
ENST00000580340.5:c.*499_*502delinsCTTG (SLC25A35)	ENSP00000464071.1:n.*499_*502delinsCTTG
ENST00000580434.5:c.103_106delinsCAAG (RANGRF)	ENSP00000462310.1:p.Gln35=
ENST00000580777.1:n.97_100delinsCAAG (RANGRF)
ENST00000581320.1:n.52_55delinsCTTG (SLC25A35)
ENST00000585311.5:c.*544_*547delinsCTTG (SLC25A35)	ENSP00000464191.1:n.*544_*547delinsCTTG
NM_001177801.1:c.103_106delinsCAAG (RANGRF)	NP_001171272.1:p.Gln35=
NM_001177802.1:c.103_106delinsCAAG (RANGRF)	NP_001171273.1:p.Gln35=
NM_016492.4:c.103_106delinsCAAG (RANGRF)	NP_057576.2:p.Gln35=
NM_201520.1:c.*632_*635delinsCTTG (SLC25A35)	NP_958928.1:n.*632_*635delinsCTTG
XM_005256618.3:c.103_106delinsCAAG (RANGRF)	XP_005256675.1:p.Gln35=
NM_001320871.1:c.*43-552_*43-549delinsCTTG (SLC25A35)	NP_001307800.1:n.*43-552_*43-549delinsCTTG
NM_001320872.1:c.*499_*502delinsCTTG (SLC25A35)	NP_001307801.1:n.*499_*502delinsCTTG
NM_001330127.1:c.103_106delinsCAAG (RANGRF)	NP_001317056.1:p.Gln35=
NM_201520.2:c.*632_*635delinsCTTG (SLC25A35)	NP_958928.1:n.*632_*635delinsCTTG
NR_135484.1:n.1956_1959delinsCTTG (SLC25A35)
NM_016492.5:c.103_106delinsCAAG (RANGRF) MANE Select	NP_057576.2:p.Gln35=
NM_001177801.2:c.103_106delinsCAAG (RANGRF)	NP_001171272.1:p.Gln35=
NM_001177802.2:c.103_106delinsCAAG (RANGRF)	NP_001171273.1:p.Gln35=
NM_001320871.2:c.*43-552_*43-549delinsCTTG (SLC25A35)	NP_001307800.1:n.*43-552_*43-549delinsCTTG
NM_001330127.2:c.103_106delinsCAAG (RANGRF)	NP_001317056.1:p.Gln35=
NM_201520.3:c.*632_*635delinsCTTG (SLC25A35)	NP_958928.1:n.*632_*635delinsCTTG
NR_135483.2:n.2177_2180delinsCTTG (SLC25A35)
NM_001320872.2:c.*499_*502delinsCTTG (SLC25A35)	NP_001307801.1:n.*499_*502delinsCTTG
NR_135484.2:n.2013_2016delinsCTTG (SLC25A35)