Canonical Allele Identifier: CA2674568794

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90703680-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703682del , CM000667.2:g.90703682del	GRCh38
NC_000005.9:g.89999499del , CM000667.1:g.89999499del	GRCh37
NC_000005.8:g.90035255del	NCBI36
NG_007083.1:g.149883del
NG_007083.2:g.179339del

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.8173del MANE Select	ENSP00000384582.2:p.His2725MetfsTer2
ENST00000639431.1:c.265+27473del	ENSP00000491057.1:n.265+27473del
ENST00000639473.1:n.3632del
ENST00000640012.1:c.1980del
ENST00000640374.1:n.1317del
ENST00000640403.1:c.5464del	ENSP00000492531.1:p.His1822MetfsTer2
ENST00000640779.1:c.2902del
ENST00000405460.6:c.8173del	ENSP00000384582.2:p.His2725MetfsTer2
ENST00000509621.1:c.870del
NM_032119.3:c.8173del	NP_115495.3:p.His2725MetfsTer2
NR_003149.1:n.8186del
XM_011543675.1:c.8170del	XP_011541977.1:p.His2724MetfsTer2
XM_011543676.1:c.8092del	XP_011541978.1:p.His2698MetfsTer2
XM_011543677.1:c.5476del	XP_011541979.1:p.His1826MetfsTer2
XM_011543678.1:c.8173del	XP_011541980.1:p.His2725MetfsTer2
XM_011543679.1:c.8173del	XP_011541981.1:p.His2725MetfsTer2
NM_032119.4:c.8173del MANE Select	NP_115495.3:p.His2725MetfsTer2
XM_017009963.2:c.8173del	XP_016865452.1:p.His2725MetfsTer2
XM_017009964.2:c.8170del	XP_016865453.1:p.His2724MetfsTer2
XM_017009965.1:c.8170del	XP_016865454.1:p.His2724MetfsTer2
XM_017009966.2:c.8092del	XP_016865455.1:p.His2698MetfsTer2
XM_017009967.1:c.8077del	XP_016865456.1:p.His2693MetfsTer2
XM_017009968.2:c.8173del	XP_016865457.1:p.His2725MetfsTer2
XM_017009969.2:c.8173del	XP_016865458.1:p.His2725MetfsTer2
XM_017009970.2:c.8173del	XP_016865459.1:p.His2725MetfsTer2
XM_017009971.2:c.8173del	XP_016865460.1:p.His2725MetfsTer2
XM_017009972.1:c.1291del	XP_016865461.1:p.His431MetfsTer2
XM_017009973.1:c.1291del	XP_016865462.1:p.His431MetfsTer2
XM_017009974.2:c.8173del	XP_016865463.1:p.His2725MetfsTer2
NR_003149.2:n.8189del