Canonical Allele Identifier: CA2246233124

Gene: RANGRF SLC25A35

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288675C= , CM000679.2:g.8288675C=	GRCh38
NC_000017.10:g.8191993C= , CM000679.1:g.8191993C=	GRCh37
NC_000017.9:g.8132718C=	NCBI36
NG_028189.1:g.5025C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.-114C= (RANGRF) MANE Select	ENSP00000226105.6:n.-114C=
ENST00000226105.10:c.-114C= (RANGRF)	ENSP00000226105.6:n.-114C=
ENST00000380067.6:c.*941G= (SLC25A35)	ENSP00000369407.2:n.*941G=
ENST00000407006.8:c.-114C= (RANGRF)	ENSP00000383940.4:n.-114C=
ENST00000579192.5:c.*43-243G= (SLC25A35)	ENSP00000462395.1:n.*43-243G=
ENST00000580434.5:c.-114C= (RANGRF)	ENSP00000462310.1:n.-114C=
ENST00000581320.1:n.91-243G= (SLC25A35)
NM_001177801.1:c.-114C= (RANGRF)	NP_001171272.1:n.-114C=
NM_001177802.1:c.-114C= (RANGRF)	NP_001171273.1:n.-114C=
NM_016492.4:c.-114C= (RANGRF)	NP_057576.2:n.-114C=
NM_201520.1:c.*941G= (SLC25A35)	NP_958928.1:n.*941G=
XM_005256618.3:c.-114C= (RANGRF)	XP_005256675.1:n.-114C=
NM_001320871.1:c.*43-243G= (SLC25A35)	NP_001307800.1:n.*43-243G=
NM_001330127.1:c.-114C= (RANGRF)	NP_001317056.1:n.-114C=
NM_201520.2:c.*941G= (SLC25A35)	NP_958928.1:n.*941G=
NM_016492.5:c.-114C= (RANGRF) MANE Select	NP_057576.2:n.-114C=
NM_001177801.2:c.-114C= (RANGRF)	NP_001171272.1:n.-114C=
NM_001177802.2:c.-114C= (RANGRF)	NP_001171273.1:n.-114C=
NM_001320871.2:c.*43-243G= (SLC25A35)	NP_001307800.1:n.*43-243G=
NM_001330127.2:c.-114C= (RANGRF)	NP_001317056.1:n.-114C=
NM_201520.3:c.*941G= (SLC25A35)	NP_958928.1:n.*941G=
NR_135483.2:n.2486G= (SLC25A35)