Canonical Allele Identifier: CA775789268

Gene: RANGRF SLC25A35

Linked Data

• dbSNP Id: rs1260346546
• gnomAD v3: 17-8288582-CGGAGCAAA-C
• gnomAD v4: 17-8288582-CGGAGCAAA-C
• MyVariant Identifiers: chr17:g.8191901_8191908del (hg19) ; chr17:g.8288583_8288590del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8288584_8288591del , CM000679.2:g.8288584_8288591del	GRCh38
NC_000017.10:g.8191902_8191909del , CM000679.1:g.8191902_8191909del	GRCh37
NC_000017.9:g.8132627_8132634del	NCBI36
NG_028189.1:g.4934_4941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226105.10:c.-205_-198del (RANGRF)	ENSP00000226105.6:n.-205_-198del
ENST00000380067.6:c.*1026_*1033del (SLC25A35)	ENSP00000369407.2:n.*1026_*1033del
ENST00000579192.5:c.*43-158_*43-151del (SLC25A35)	ENSP00000462395.1:n.*43-158_*43-151del
ENST00000581320.1:n.91-158_91-151del (SLC25A35)
NM_201520.1:c.*1026_*1033del (SLC25A35)	NP_958928.1:n.*1026_*1033del
XM_005256618.3:c.-205_-198del (RANGRF)	XP_005256675.1:n.-205_-198del
NM_001320871.1:c.*43-158_*43-151del (SLC25A35)	NP_001307800.1:n.*43-158_*43-151del
NM_001330127.1:c.-205_-198del (RANGRF)	NP_001317056.1:n.-205_-198del
NM_201520.2:c.*1026_*1033del (SLC25A35)	NP_958928.1:n.*1026_*1033del
NM_001320871.2:c.*43-158_*43-151del (SLC25A35)	NP_001307800.1:n.*43-158_*43-151del
NM_201520.3:c.*1026_*1033del (SLC25A35)	NP_958928.1:n.*1026_*1033del
NR_135483.2:n.2571_2578del (SLC25A35)