Canonical Allele Identifier: CA497776870

Gene: RANGRF SLC25A35

Linked Data

• MyVariant Identifiers: chr17:g.8192148T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288830T>C , CM000679.2:g.8288830T>C	GRCh38
NC_000017.10:g.8192148T>C , CM000679.1:g.8192148T>C	GRCh37
NC_000017.9:g.8132873T>C	NCBI36
NG_028189.1:g.5180T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.42T>C (RANGRF) MANE Select	ENSP00000226105.6:p.Phe14=
ENST00000226105.10:c.42T>C (RANGRF)	ENSP00000226105.6:p.Phe14=
ENST00000380067.6:c.*786A>G (SLC25A35)	ENSP00000369407.2:n.*786A>G
ENST00000407006.8:c.42T>C (RANGRF)	ENSP00000383940.4:p.Phe14=
ENST00000439238.3:c.42T>C (RANGRF)	ENSP00000413190.3:p.Phe14=
ENST00000578849.1:n.132T>C (RANGRF)
ENST00000579192.5:c.*43-398A>G (SLC25A35)	ENSP00000462395.1:n.*43-398A>G
ENST00000580434.5:c.42T>C (RANGRF)	ENSP00000462310.1:p.Phe14=
ENST00000581320.1:n.90+116A>G (SLC25A35)
NM_001177801.1:c.42T>C (RANGRF)	NP_001171272.1:p.Phe14=
NM_001177802.1:c.42T>C (RANGRF)	NP_001171273.1:p.Phe14=
NM_016492.4:c.42T>C (RANGRF)	NP_057576.2:p.Phe14=
NM_201520.1:c.*786A>G (SLC25A35)	NP_958928.1:n.*786A>G
XM_005256618.3:c.42T>C (RANGRF)	XP_005256675.1:p.Phe14=
NM_001320871.1:c.*43-398A>G (SLC25A35)	NP_001307800.1:n.*43-398A>G
NM_001330127.1:c.42T>C (RANGRF)	NP_001317056.1:p.Phe14=
NM_201520.2:c.*786A>G (SLC25A35)	NP_958928.1:n.*786A>G
NM_016492.5:c.42T>C (RANGRF) MANE Select	NP_057576.2:p.Phe14=
NM_001177801.2:c.42T>C (RANGRF)	NP_001171272.1:p.Phe14=
NM_001177802.2:c.42T>C (RANGRF)	NP_001171273.1:p.Phe14=
NM_001320871.2:c.*43-398A>G (SLC25A35)	NP_001307800.1:n.*43-398A>G
NM_001330127.2:c.42T>C (RANGRF)	NP_001317056.1:p.Phe14=
NM_201520.3:c.*786A>G (SLC25A35)	NP_958928.1:n.*786A>G
NR_135483.2:n.2331A>G (SLC25A35)