Canonical Allele Identifier: CA2246233530

Gene: RANGRF SLC25A35

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8289001C= , CM000679.2:g.8289001C=	GRCh38
NC_000017.10:g.8192319C= , CM000679.1:g.8192319C=	GRCh37
NC_000017.9:g.8133044C=	NCBI36
NG_028189.1:g.5351C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.123C= (RANGRF) MANE Select	ENSP00000226105.6:p.Pro41=
ENST00000226105.10:c.123C= (RANGRF)	ENSP00000226105.6:p.Pro41=
ENST00000380067.6:c.*615G= (SLC25A35)	ENSP00000369407.2:n.*615G=
ENST00000407006.8:c.123C= (RANGRF)	ENSP00000383940.4:p.Pro41=
ENST00000439238.3:c.123C= (RANGRF)	ENSP00000413190.3:p.Pro41=
ENST00000578849.1:n.213C= (RANGRF)
ENST00000579192.5:c.*43-569G= (SLC25A35)	ENSP00000462395.1:n.*43-569G=
ENST00000580340.5:c.*482G= (SLC25A35)	ENSP00000464071.1:n.*482G=
ENST00000580434.5:c.123C= (RANGRF)	ENSP00000462310.1:p.Pro41=
ENST00000580777.1:n.117C= (RANGRF)
ENST00000581320.1:n.35G= (SLC25A35)
ENST00000585311.5:c.*527G= (SLC25A35)	ENSP00000464191.1:n.*527G=
NM_001177801.1:c.123C= (RANGRF)	NP_001171272.1:p.Pro41=
NM_001177802.1:c.123C= (RANGRF)	NP_001171273.1:p.Pro41=
NM_016492.4:c.123C= (RANGRF)	NP_057576.2:p.Pro41=
NM_201520.1:c.*615G= (SLC25A35)	NP_958928.1:n.*615G=
XM_005256618.3:c.123C= (RANGRF)	XP_005256675.1:p.Pro41=
NM_001320871.1:c.*43-569G= (SLC25A35)	NP_001307800.1:n.*43-569G=
NM_001320872.1:c.*482G= (SLC25A35)	NP_001307801.1:n.*482G=
NM_001330127.1:c.123C= (RANGRF)	NP_001317056.1:p.Pro41=
NM_201520.2:c.*615G= (SLC25A35)	NP_958928.1:n.*615G=
NR_135484.1:n.1939G= (SLC25A35)
NM_016492.5:c.123C= (RANGRF) MANE Select	NP_057576.2:p.Pro41=
NM_001177801.2:c.123C= (RANGRF)	NP_001171272.1:p.Pro41=
NM_001177802.2:c.123C= (RANGRF)	NP_001171273.1:p.Pro41=
NM_001320871.2:c.*43-569G= (SLC25A35)	NP_001307800.1:n.*43-569G=
NM_001330127.2:c.123C= (RANGRF)	NP_001317056.1:p.Pro41=
NM_201520.3:c.*615G= (SLC25A35)	NP_958928.1:n.*615G=
NR_135483.2:n.2160G= (SLC25A35)
NM_001320872.2:c.*482G= (SLC25A35)	NP_001307801.1:n.*482G=
NR_135484.2:n.1996G= (SLC25A35)