Canonical Allele Identifier: CA2246233491

Gene: RANGRF SLC25A35

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288964G= , CM000679.2:g.8288964G=	GRCh38
NC_000017.10:g.8192282G= , CM000679.1:g.8192282G=	GRCh37
NC_000017.9:g.8133007G=	NCBI36
NG_028189.1:g.5314G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.86G= (RANGRF) MANE Select	ENSP00000226105.6:p.Arg29=
ENST00000226105.10:c.86G= (RANGRF)	ENSP00000226105.6:p.Arg29=
ENST00000380067.6:c.*652C= (SLC25A35)	ENSP00000369407.2:n.*652C=
ENST00000407006.8:c.86G= (RANGRF)	ENSP00000383940.4:p.Arg29=
ENST00000439238.3:c.86G= (RANGRF)	ENSP00000413190.3:p.Arg29=
ENST00000578849.1:n.176G= (RANGRF)
ENST00000579192.5:c.*43-532C= (SLC25A35)	ENSP00000462395.1:n.*43-532C=
ENST00000580340.5:c.*519C= (SLC25A35)	ENSP00000464071.1:n.*519C=
ENST00000580434.5:c.86G= (RANGRF)	ENSP00000462310.1:p.Arg29=
ENST00000580777.1:n.80G= (RANGRF)
ENST00000581320.1:n.72C= (SLC25A35)
ENST00000585311.5:c.*564C= (SLC25A35)	ENSP00000464191.1:n.*564C=
NM_001177801.1:c.86G= (RANGRF)	NP_001171272.1:p.Arg29=
NM_001177802.1:c.86G= (RANGRF)	NP_001171273.1:p.Arg29=
NM_016492.4:c.86G= (RANGRF)	NP_057576.2:p.Arg29=
NM_201520.1:c.*652C= (SLC25A35)	NP_958928.1:n.*652C=
XM_005256618.3:c.86G= (RANGRF)	XP_005256675.1:p.Arg29=
NM_001320871.1:c.*43-532C= (SLC25A35)	NP_001307800.1:n.*43-532C=
NM_001320872.1:c.*519C= (SLC25A35)	NP_001307801.1:n.*519C=
NM_001330127.1:c.86G= (RANGRF)	NP_001317056.1:p.Arg29=
NM_201520.2:c.*652C= (SLC25A35)	NP_958928.1:n.*652C=
NR_135484.1:n.1976C= (SLC25A35)
NM_016492.5:c.86G= (RANGRF) MANE Select	NP_057576.2:p.Arg29=
NM_001177801.2:c.86G= (RANGRF)	NP_001171272.1:p.Arg29=
NM_001177802.2:c.86G= (RANGRF)	NP_001171273.1:p.Arg29=
NM_001320871.2:c.*43-532C= (SLC25A35)	NP_001307800.1:n.*43-532C=
NM_001330127.2:c.86G= (RANGRF)	NP_001317056.1:p.Arg29=
NM_201520.3:c.*652C= (SLC25A35)	NP_958928.1:n.*652C=
NR_135483.2:n.2197C= (SLC25A35)
NM_001320872.2:c.*519C= (SLC25A35)	NP_001307801.1:n.*519C=
NR_135484.2:n.2033C= (SLC25A35)