Canonical Allele Identifier: CA626350464

Gene: ARL17B LRRC37A

Linked Data

• dbSNP Id: rs891135752
• gnomAD v2: 17-44355775-TTTGTTG-T
• gnomAD v3: 17-46278409-TTTGTTG-T
• gnomAD v4: 17-46278409-TTTGTTG-T
• MyVariant Identifiers: chr17:g.44355776_44355781del (hg19) ; chr17:g.46278410_46278415del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46278415_46278420del , CM000679.2:g.46278415_46278420del	GRCh38
NC_000017.10:g.44355781_44355786del , CM000679.1:g.44355781_44355786del	GRCh37
NC_000017.9:g.41711558_41711563del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705759.1:n.377-2997_377-2992del (ARL17B)
ENST00000570618.5:c.*22-2997_*22-2992del (ARL17B)	ENSP00000459151.1:n.*22-2997_*22-2992del
XM_005256918.3:c.*22-2997_*22-2992del (ARL17B)	XP_005256975.1:n.*22-2997_*22-2992del
XM_005257887.3:c.27-21379_27-21374del (LRRC37A)	XP_005257944.1:n.27-21379_27-21374del
XM_011524162.1:c.*54-2997_*54-2992del (ARL17B)	XP_011522464.1:n.*54-2997_*54-2992del
XM_011525540.1:c.27-21379_27-21374del (LRRC37A)	XP_011523842.1:n.27-21379_27-21374del
NM_001103154.2:c.*22-2997_*22-2992del (ARL17B)	NP_001096624.1:n.*22-2997_*22-2992del
XM_011524162.3:c.*54-2997_*54-2992del (ARL17B)	XP_011522464.1:n.*54-2997_*54-2992del