Canonical Allele Identifier: CA624735994

Gene: RANGRF SLC25A35

Linked Data

• dbSNP Id: rs1466497858
• gnomAD v2: 17-8191916-A-AC
• gnomAD v3: 17-8288598-A-AC
• gnomAD v4: 17-8288598-A-AC
• MyVariant Identifiers: chr17:g.8191916_8191917insC (hg19) ; chr17:g.8288598_8288599insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288603dup , CM000679.2:g.8288603dup	GRCh38
NC_000017.10:g.8191921dup , CM000679.1:g.8191921dup	GRCh37
NC_000017.9:g.8132646dup	NCBI36
NG_028189.1:g.4953dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-186dup (RANGRF)	ENSP00000226105.6:n.-186dup
ENST00000380067.6:c.*1017dup (SLC25A35)	ENSP00000369407.2:n.*1017dup
ENST00000579192.5:c.*43-167dup (SLC25A35)	ENSP00000462395.1:n.*43-167dup
ENST00000581320.1:n.91-167dup (SLC25A35)
NM_201520.1:c.*1017dup (SLC25A35)	NP_958928.1:n.*1017dup
XM_005256618.3:c.-186dup (RANGRF)	XP_005256675.1:n.-186dup
NM_001320871.1:c.*43-167dup (SLC25A35)	NP_001307800.1:n.*43-167dup
NM_001330127.1:c.-186dup (RANGRF)	NP_001317056.1:n.-186dup
NM_201520.2:c.*1017dup (SLC25A35)	NP_958928.1:n.*1017dup
NM_001320871.2:c.*43-167dup (SLC25A35)	NP_001307800.1:n.*43-167dup
NM_201520.3:c.*1017dup (SLC25A35)	NP_958928.1:n.*1017dup
NR_135483.2:n.2562dup (SLC25A35)