Canonical Allele Identifier: CA497776806

Gene: RANGRF SLC25A35

Linked Data

• MyVariant Identifiers: chr17:g.8192131C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288813C>T , CM000679.2:g.8288813C>T	GRCh38
NC_000017.10:g.8192131C>T , CM000679.1:g.8192131C>T	GRCh37
NC_000017.9:g.8132856C>T	NCBI36
NG_028189.1:g.5163C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.25C>T (RANGRF) MANE Select	ENSP00000226105.6:p.Leu9=
ENST00000226105.10:c.25C>T (RANGRF)	ENSP00000226105.6:p.Leu9=
ENST00000380067.6:c.*803G>A (SLC25A35)	ENSP00000369407.2:n.*803G>A
ENST00000407006.8:c.25C>T (RANGRF)	ENSP00000383940.4:p.Leu9=
ENST00000439238.3:c.25C>T (RANGRF)	ENSP00000413190.3:p.Leu9=
ENST00000578849.1:n.115C>T (RANGRF)
ENST00000579192.5:c.*43-381G>A (SLC25A35)	ENSP00000462395.1:n.*43-381G>A
ENST00000580434.5:c.25C>T (RANGRF)	ENSP00000462310.1:p.Leu9=
ENST00000581320.1:n.90+133G>A (SLC25A35)
NM_001177801.1:c.25C>T (RANGRF)	NP_001171272.1:p.Leu9=
NM_001177802.1:c.25C>T (RANGRF)	NP_001171273.1:p.Leu9=
NM_016492.4:c.25C>T (RANGRF)	NP_057576.2:p.Leu9=
NM_201520.1:c.*803G>A (SLC25A35)	NP_958928.1:n.*803G>A
XM_005256618.3:c.25C>T (RANGRF)	XP_005256675.1:p.Leu9=
NM_001320871.1:c.*43-381G>A (SLC25A35)	NP_001307800.1:n.*43-381G>A
NM_001330127.1:c.25C>T (RANGRF)	NP_001317056.1:p.Leu9=
NM_201520.2:c.*803G>A (SLC25A35)	NP_958928.1:n.*803G>A
NM_016492.5:c.25C>T (RANGRF) MANE Select	NP_057576.2:p.Leu9=
NM_001177801.2:c.25C>T (RANGRF)	NP_001171272.1:p.Leu9=
NM_001177802.2:c.25C>T (RANGRF)	NP_001171273.1:p.Leu9=
NM_001320871.2:c.*43-381G>A (SLC25A35)	NP_001307800.1:n.*43-381G>A
NM_001330127.2:c.25C>T (RANGRF)	NP_001317056.1:p.Leu9=
NM_201520.3:c.*803G>A (SLC25A35)	NP_958928.1:n.*803G>A
NR_135483.2:n.2348G>A (SLC25A35)