Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8289103C= , CM000679.2:g.8289103C=	GRCh38
NC_000017.10:g.8192421C= , CM000679.1:g.8192421C=	GRCh37
NC_000017.9:g.8133146C=	NCBI36
NG_028189.1:g.5453C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.194+31C= (RANGRF) MANE Select	ENSP00000226105.6:n.194+31C=
ENST00000226105.10:c.194+31C= (RANGRF)	ENSP00000226105.6:n.194+31C=
ENST00000380067.6:c.*513G= (SLC25A35)	ENSP00000369407.2:n.*513G=
ENST00000407006.8:c.194+31C= (RANGRF)	ENSP00000383940.4:n.194+31C=
ENST00000439238.3:c.194+31C= (RANGRF)	ENSP00000413190.3:n.194+31C=
ENST00000578849.1:n.315C= (RANGRF)
ENST00000579192.5:c.*42+471G= (SLC25A35)	ENSP00000462395.1:n.*42+471G=
ENST00000580340.5:c.*380G= (SLC25A35)	ENSP00000464071.1:n.*380G=
ENST00000580434.5:c.194+31C= (RANGRF)	ENSP00000462310.1:n.194+31C=
ENST00000580777.1:n.188+31C= (RANGRF)
ENST00000585311.5:c.*425G= (SLC25A35)	ENSP00000464191.1:n.*425G=
NM_001177801.1:c.194+31C= (RANGRF)	NP_001171272.1:n.194+31C=
NM_001177802.1:c.194+31C= (RANGRF)	NP_001171273.1:n.194+31C=
NM_016492.4:c.194+31C= (RANGRF)	NP_057576.2:n.194+31C=
NM_201520.1:c.*513G= (SLC25A35)	NP_958928.1:n.*513G=
XM_005256618.3:c.194+31C= (RANGRF)	XP_005256675.1:n.194+31C=
NM_001320871.1:c.*42+471G= (SLC25A35)	NP_001307800.1:n.*42+471G=
NM_001320872.1:c.*380G= (SLC25A35)	NP_001307801.1:n.*380G=
NM_001330127.1:c.194+31C= (RANGRF)	NP_001317056.1:n.194+31C=
NM_201520.2:c.*513G= (SLC25A35)	NP_958928.1:n.*513G=
NR_135484.1:n.1837G= (SLC25A35)
NM_016492.5:c.194+31C= (RANGRF) MANE Select	NP_057576.2:n.194+31C=
NM_001177801.2:c.194+31C= (RANGRF)	NP_001171272.1:n.194+31C=
NM_001177802.2:c.194+31C= (RANGRF)	NP_001171273.1:n.194+31C=
NM_001320871.2:c.*42+471G= (SLC25A35)	NP_001307800.1:n.*42+471G=
NM_001330127.2:c.194+31C= (RANGRF)	NP_001317056.1:n.194+31C=
NM_201520.3:c.*513G= (SLC25A35)	NP_958928.1:n.*513G=
NR_135483.2:n.2058G= (SLC25A35)
NM_001320872.2:c.*380G= (SLC25A35)	NP_001307801.1:n.*380G=
NR_135484.2:n.1894G= (SLC25A35)