Canonical Allele Identifier: CA2246233555

Gene: RANGRF SLC25A35

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8289025G= , CM000679.2:g.8289025G=	GRCh38
NC_000017.10:g.8192343G= , CM000679.1:g.8192343G=	GRCh37
NC_000017.9:g.8133068G=	NCBI36
NG_028189.1:g.5375G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.147G= (RANGRF) MANE Select	ENSP00000226105.6:p.Val49=
ENST00000226105.10:c.147G= (RANGRF)	ENSP00000226105.6:p.Val49=
ENST00000380067.6:c.*591C= (SLC25A35)	ENSP00000369407.2:n.*591C=
ENST00000407006.8:c.147G= (RANGRF)	ENSP00000383940.4:p.Val49=
ENST00000439238.3:c.147G= (RANGRF)	ENSP00000413190.3:p.Val49=
ENST00000578849.1:n.237G= (RANGRF)
ENST00000579192.5:c.*42+549C= (SLC25A35)	ENSP00000462395.1:n.*42+549C=
ENST00000580340.5:c.*458C= (SLC25A35)	ENSP00000464071.1:n.*458C=
ENST00000580434.5:c.147G= (RANGRF)	ENSP00000462310.1:p.Val49=
ENST00000580777.1:n.141G= (RANGRF)
ENST00000581320.1:n.11C= (SLC25A35)
ENST00000585311.5:c.*503C= (SLC25A35)	ENSP00000464191.1:n.*503C=
NM_001177801.1:c.147G= (RANGRF)	NP_001171272.1:p.Val49=
NM_001177802.1:c.147G= (RANGRF)	NP_001171273.1:p.Val49=
NM_016492.4:c.147G= (RANGRF)	NP_057576.2:p.Val49=
NM_201520.1:c.*591C= (SLC25A35)	NP_958928.1:n.*591C=
XM_005256618.3:c.147G= (RANGRF)	XP_005256675.1:p.Val49=
NM_001320871.1:c.*42+549C= (SLC25A35)	NP_001307800.1:n.*42+549C=
NM_001320872.1:c.*458C= (SLC25A35)	NP_001307801.1:n.*458C=
NM_001330127.1:c.147G= (RANGRF)	NP_001317056.1:p.Val49=
NM_201520.2:c.*591C= (SLC25A35)	NP_958928.1:n.*591C=
NR_135484.1:n.1915C= (SLC25A35)
NM_016492.5:c.147G= (RANGRF) MANE Select	NP_057576.2:p.Val49=
NM_001177801.2:c.147G= (RANGRF)	NP_001171272.1:p.Val49=
NM_001177802.2:c.147G= (RANGRF)	NP_001171273.1:p.Val49=
NM_001320871.2:c.*42+549C= (SLC25A35)	NP_001307800.1:n.*42+549C=
NM_001330127.2:c.147G= (RANGRF)	NP_001317056.1:p.Val49=
NM_201520.3:c.*591C= (SLC25A35)	NP_958928.1:n.*591C=
NR_135483.2:n.2136C= (SLC25A35)
NM_001320872.2:c.*458C= (SLC25A35)	NP_001307801.1:n.*458C=
NR_135484.2:n.1972C= (SLC25A35)