Canonical Allele Identifier: CA2246233533

Gene: RANGRF SLC25A35

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8289002G= , CM000679.2:g.8289002G=	GRCh38
NC_000017.10:g.8192320G= , CM000679.1:g.8192320G=	GRCh37
NC_000017.9:g.8133045G=	NCBI36
NG_028189.1:g.5352G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.124G= (RANGRF) MANE Select	ENSP00000226105.6:p.Val42=
ENST00000226105.10:c.124G= (RANGRF)	ENSP00000226105.6:p.Val42=
ENST00000380067.6:c.*614C= (SLC25A35)	ENSP00000369407.2:n.*614C=
ENST00000407006.8:c.124G= (RANGRF)	ENSP00000383940.4:p.Val42=
ENST00000439238.3:c.124G= (RANGRF)	ENSP00000413190.3:p.Val42=
ENST00000578849.1:n.214G= (RANGRF)
ENST00000579192.5:c.*43-570C= (SLC25A35)	ENSP00000462395.1:n.*43-570C=
ENST00000580340.5:c.*481C= (SLC25A35)	ENSP00000464071.1:n.*481C=
ENST00000580434.5:c.124G= (RANGRF)	ENSP00000462310.1:p.Val42=
ENST00000580777.1:n.118G= (RANGRF)
ENST00000581320.1:n.34C= (SLC25A35)
ENST00000585311.5:c.*526C= (SLC25A35)	ENSP00000464191.1:n.*526C=
NM_001177801.1:c.124G= (RANGRF)	NP_001171272.1:p.Val42=
NM_001177802.1:c.124G= (RANGRF)	NP_001171273.1:p.Val42=
NM_016492.4:c.124G= (RANGRF)	NP_057576.2:p.Val42=
NM_201520.1:c.*614C= (SLC25A35)	NP_958928.1:n.*614C=
XM_005256618.3:c.124G= (RANGRF)	XP_005256675.1:p.Val42=
NM_001320871.1:c.*43-570C= (SLC25A35)	NP_001307800.1:n.*43-570C=
NM_001320872.1:c.*481C= (SLC25A35)	NP_001307801.1:n.*481C=
NM_001330127.1:c.124G= (RANGRF)	NP_001317056.1:p.Val42=
NM_201520.2:c.*614C= (SLC25A35)	NP_958928.1:n.*614C=
NR_135484.1:n.1938C= (SLC25A35)
NM_016492.5:c.124G= (RANGRF) MANE Select	NP_057576.2:p.Val42=
NM_001177801.2:c.124G= (RANGRF)	NP_001171272.1:p.Val42=
NM_001177802.2:c.124G= (RANGRF)	NP_001171273.1:p.Val42=
NM_001320871.2:c.*43-570C= (SLC25A35)	NP_001307800.1:n.*43-570C=
NM_001330127.2:c.124G= (RANGRF)	NP_001317056.1:p.Val42=
NM_201520.3:c.*614C= (SLC25A35)	NP_958928.1:n.*614C=
NR_135483.2:n.2159C= (SLC25A35)
NM_001320872.2:c.*481C= (SLC25A35)	NP_001307801.1:n.*481C=
NR_135484.2:n.1995C= (SLC25A35)