Canonical Allele Identifier: CA656419781

Gene: RANGRF SLC25A35

Linked Data

• COSMIC: COSN23404821

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288594_8288595insT , CM000679.2:g.8288594_8288595insT	GRCh38
NC_000017.10:g.8191912_8191913insT , CM000679.1:g.8191912_8191913insT	GRCh37
NC_000017.9:g.8132637_8132638insT	NCBI36
NG_028189.1:g.4944_4945insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-195_-194insT (RANGRF)	ENSP00000226105.6:n.-195_-194insT
ENST00000380067.6:c.*1021_*1022insA (SLC25A35)	ENSP00000369407.2:n.*1021_*1022insA
ENST00000579192.5:c.*43-163_*43-162insA (SLC25A35)	ENSP00000462395.1:n.*43-163_*43-162insA
ENST00000581320.1:n.91-163_91-162insA (SLC25A35)
NM_201520.1:c.*1021_*1022insA (SLC25A35)	NP_958928.1:n.*1021_*1022insA
XM_005256618.3:c.-195_-194insT (RANGRF)	XP_005256675.1:n.-195_-194insT
NM_001320871.1:c.*43-163_*43-162insA (SLC25A35)	NP_001307800.1:n.*43-163_*43-162insA
NM_001330127.1:c.-195_-194insT (RANGRF)	NP_001317056.1:n.-195_-194insT
NM_201520.2:c.*1021_*1022insA (SLC25A35)	NP_958928.1:n.*1021_*1022insA
NM_001320871.2:c.*43-163_*43-162insA (SLC25A35)	NP_001307800.1:n.*43-163_*43-162insA
NM_201520.3:c.*1021_*1022insA (SLC25A35)	NP_958928.1:n.*1021_*1022insA
NR_135483.2:n.2566_2567insA (SLC25A35)