Canonical Allele Identifier: CA2601020019
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs2149629235

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692191_90692194del , CM000667.2:g.90692191_90692194del GRCh38
NC_000005.9:g.89988008_89988011del , CM000667.1:g.89988008_89988011del GRCh37
NC_000005.8:g.90023764_90023767del NCBI36
NG_007083.1:g.138392_138395del
NG_007083.2:g.167848_167851del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.6952-414_6952-411del MANE Select ENSP00000384582.2:n.6952-414_6952-411del
ENST00000639431.1:c.265+15982_265+15985del ENSP00000491057.1:n.265+15982_265+15985del
ENST00000639473.1:n.2411-414_2411-411del
ENST00000640012.1:c.759-414_759-411del
ENST00000640374.1:n.96-414_96-411del
ENST00000640403.1:c.4243-414_4243-411del ENSP00000492531.1:n.4243-414_4243-411del
ENST00000640779.1:c.1681-414_1681-411del
ENST00000405460.6:c.6952-414_6952-411del ENSP00000384582.2:n.6952-414_6952-411del
NM_032119.3:c.6952-414_6952-411del NP_115495.3:n.6952-414_6952-411del
NR_003149.1:n.6965-414_6965-411del
XM_011543675.1:c.6949-414_6949-411del XP_011541977.1:n.6949-414_6949-411del
XM_011543676.1:c.6871-414_6871-411del XP_011541978.1:n.6871-414_6871-411del
XM_011543677.1:c.4255-414_4255-411del XP_011541979.1:n.4255-414_4255-411del
XM_011543678.1:c.6952-414_6952-411del XP_011541980.1:n.6952-414_6952-411del
XM_011543679.1:c.6952-414_6952-411del XP_011541981.1:n.6952-414_6952-411del
NM_032119.4:c.6952-414_6952-411del MANE Select NP_115495.3:n.6952-414_6952-411del
XM_017009963.2:c.6952-414_6952-411del XP_016865452.1:n.6952-414_6952-411del
XM_017009964.2:c.6949-414_6949-411del XP_016865453.1:n.6949-414_6949-411del
XM_017009965.1:c.6949-414_6949-411del XP_016865454.1:n.6949-414_6949-411del
XM_017009966.2:c.6871-414_6871-411del XP_016865455.1:n.6871-414_6871-411del
XM_017009967.1:c.6856-414_6856-411del XP_016865456.1:n.6856-414_6856-411del
XM_017009968.2:c.6952-414_6952-411del XP_016865457.1:n.6952-414_6952-411del
XM_017009969.2:c.6952-414_6952-411del XP_016865458.1:n.6952-414_6952-411del
XM_017009970.2:c.6952-414_6952-411del XP_016865459.1:n.6952-414_6952-411del
XM_017009971.2:c.6952-414_6952-411del XP_016865460.1:n.6952-414_6952-411del
XM_017009972.1:c.70-414_70-411del XP_016865461.1:n.70-414_70-411del
XM_017009973.1:c.70-414_70-411del XP_016865462.1:n.70-414_70-411del
XM_017009974.2:c.6952-414_6952-411del XP_016865463.1:n.6952-414_6952-411del
NR_003149.2:n.6968-414_6968-411del