Canonical Allele Identifier: CA2246233231

Gene: RANGRF SLC25A35

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288775C= , CM000679.2:g.8288775C=	GRCh38
NC_000017.10:g.8192093C= , CM000679.1:g.8192093C=	GRCh37
NC_000017.9:g.8132818C=	NCBI36
NG_028189.1:g.5125C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.-14C= (RANGRF) MANE Select	ENSP00000226105.6:n.-14C=
ENST00000226105.10:c.-14C= (RANGRF)	ENSP00000226105.6:n.-14C=
ENST00000380067.6:c.*841G= (SLC25A35)	ENSP00000369407.2:n.*841G=
ENST00000407006.8:c.-14C= (RANGRF)	ENSP00000383940.4:n.-14C=
ENST00000439238.3:c.-14C= (RANGRF)	ENSP00000413190.3:n.-14C=
ENST00000578849.1:n.77C= (RANGRF)
ENST00000579192.5:c.*43-343G= (SLC25A35)	ENSP00000462395.1:n.*43-343G=
ENST00000580434.5:c.-14C= (RANGRF)	ENSP00000462310.1:n.-14C=
ENST00000581320.1:n.90+171G= (SLC25A35)
NM_001177801.1:c.-14C= (RANGRF)	NP_001171272.1:n.-14C=
NM_001177802.1:c.-14C= (RANGRF)	NP_001171273.1:n.-14C=
NM_016492.4:c.-14C= (RANGRF)	NP_057576.2:n.-14C=
NM_201520.1:c.*841G= (SLC25A35)	NP_958928.1:n.*841G=
XM_005256618.3:c.-14C= (RANGRF)	XP_005256675.1:n.-14C=
NM_001320871.1:c.*43-343G= (SLC25A35)	NP_001307800.1:n.*43-343G=
NM_001330127.1:c.-14C= (RANGRF)	NP_001317056.1:n.-14C=
NM_201520.2:c.*841G= (SLC25A35)	NP_958928.1:n.*841G=
NM_016492.5:c.-14C= (RANGRF) MANE Select	NP_057576.2:n.-14C=
NM_001177801.2:c.-14C= (RANGRF)	NP_001171272.1:n.-14C=
NM_001177802.2:c.-14C= (RANGRF)	NP_001171273.1:n.-14C=
NM_001320871.2:c.*43-343G= (SLC25A35)	NP_001307800.1:n.*43-343G=
NM_001330127.2:c.-14C= (RANGRF)	NP_001317056.1:n.-14C=
NM_201520.3:c.*841G= (SLC25A35)	NP_958928.1:n.*841G=
NR_135483.2:n.2386G= (SLC25A35)