Canonical Allele Identifier: CA497777153

Gene: RANGRF SLC25A35

Linked Data

• MyVariant Identifiers: chr17:g.8192310C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288992C>T , CM000679.2:g.8288992C>T	GRCh38
NC_000017.10:g.8192310C>T , CM000679.1:g.8192310C>T	GRCh37
NC_000017.9:g.8133035C>T	NCBI36
NG_028189.1:g.5342C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.11:c.114C>T (RANGRF) MANE Select	ENSP00000226105.6:p.Phe38=
ENST00000226105.10:c.114C>T (RANGRF)	ENSP00000226105.6:p.Phe38=
ENST00000380067.6:c.*624G>A (SLC25A35)	ENSP00000369407.2:n.*624G>A
ENST00000407006.8:c.114C>T (RANGRF)	ENSP00000383940.4:p.Phe38=
ENST00000439238.3:c.114C>T (RANGRF)	ENSP00000413190.3:p.Phe38=
ENST00000578849.1:n.204C>T (RANGRF)
ENST00000579192.5:c.*43-560G>A (SLC25A35)	ENSP00000462395.1:n.*43-560G>A
ENST00000580340.5:c.*491G>A (SLC25A35)	ENSP00000464071.1:n.*491G>A
ENST00000580434.5:c.114C>T (RANGRF)	ENSP00000462310.1:p.Phe38=
ENST00000580777.1:n.108C>T (RANGRF)
ENST00000581320.1:n.44G>A (SLC25A35)
ENST00000585311.5:c.*536G>A (SLC25A35)	ENSP00000464191.1:n.*536G>A
NM_001177801.1:c.114C>T (RANGRF)	NP_001171272.1:p.Phe38=
NM_001177802.1:c.114C>T (RANGRF)	NP_001171273.1:p.Phe38=
NM_016492.4:c.114C>T (RANGRF)	NP_057576.2:p.Phe38=
NM_201520.1:c.*624G>A (SLC25A35)	NP_958928.1:n.*624G>A
XM_005256618.3:c.114C>T (RANGRF)	XP_005256675.1:p.Phe38=
NM_001320871.1:c.*43-560G>A (SLC25A35)	NP_001307800.1:n.*43-560G>A
NM_001320872.1:c.*491G>A (SLC25A35)	NP_001307801.1:n.*491G>A
NM_001330127.1:c.114C>T (RANGRF)	NP_001317056.1:p.Phe38=
NM_201520.2:c.*624G>A (SLC25A35)	NP_958928.1:n.*624G>A
NR_135484.1:n.1948G>A (SLC25A35)
NM_016492.5:c.114C>T (RANGRF) MANE Select	NP_057576.2:p.Phe38=
NM_001177801.2:c.114C>T (RANGRF)	NP_001171272.1:p.Phe38=
NM_001177802.2:c.114C>T (RANGRF)	NP_001171273.1:p.Phe38=
NM_001320871.2:c.*43-560G>A (SLC25A35)	NP_001307800.1:n.*43-560G>A
NM_001330127.2:c.114C>T (RANGRF)	NP_001317056.1:p.Phe38=
NM_201520.3:c.*624G>A (SLC25A35)	NP_958928.1:n.*624G>A
NR_135483.2:n.2169G>A (SLC25A35)
NM_001320872.2:c.*491G>A (SLC25A35)	NP_001307801.1:n.*491G>A
NR_135484.2:n.2005G>A (SLC25A35)