Canonical Allele Identifier: CA2767420654
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692938_90692939del , CM000667.2:g.90692938_90692939del GRCh38
NC_000005.9:g.89988755_89988756del , CM000667.1:g.89988755_89988756del GRCh37
NC_000005.8:g.90024511_90024512del NCBI36
NG_007083.1:g.139139_139140del
NG_007083.2:g.168595_168596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7133+152_7133+153del MANE Select ENSP00000384582.2:n.7133+152_7133+153del
ENST00000639431.1:c.265+16729_265+16730del ENSP00000491057.1:n.265+16729_265+16730del
ENST00000639473.1:n.2592+152_2592+153del
ENST00000640012.1:c.940+152_940+153del
ENST00000640374.1:n.277+152_277+153del
ENST00000640403.1:c.4424+152_4424+153del ENSP00000492531.1:n.4424+152_4424+153del
ENST00000640779.1:c.1862+152_1862+153del
ENST00000405460.6:c.7133+152_7133+153del ENSP00000384582.2:n.7133+152_7133+153del
NM_032119.3:c.7133+152_7133+153del NP_115495.3:n.7133+152_7133+153del
NR_003149.1:n.7146+152_7146+153del
XM_011543675.1:c.7130+152_7130+153del XP_011541977.1:n.7130+152_7130+153del
XM_011543676.1:c.7052+152_7052+153del XP_011541978.1:n.7052+152_7052+153del
XM_011543677.1:c.4436+152_4436+153del XP_011541979.1:n.4436+152_4436+153del
XM_011543678.1:c.7133+152_7133+153del XP_011541980.1:n.7133+152_7133+153del
XM_011543679.1:c.7133+152_7133+153del XP_011541981.1:n.7133+152_7133+153del
NM_032119.4:c.7133+152_7133+153del MANE Select NP_115495.3:n.7133+152_7133+153del
XM_017009963.2:c.7133+152_7133+153del XP_016865452.1:n.7133+152_7133+153del
XM_017009964.2:c.7130+152_7130+153del XP_016865453.1:n.7130+152_7130+153del
XM_017009965.1:c.7130+152_7130+153del XP_016865454.1:n.7130+152_7130+153del
XM_017009966.2:c.7052+152_7052+153del XP_016865455.1:n.7052+152_7052+153del
XM_017009967.1:c.7037+152_7037+153del XP_016865456.1:n.7037+152_7037+153del
XM_017009968.2:c.7133+152_7133+153del XP_016865457.1:n.7133+152_7133+153del
XM_017009969.2:c.7133+152_7133+153del XP_016865458.1:n.7133+152_7133+153del
XM_017009970.2:c.7133+152_7133+153del XP_016865459.1:n.7133+152_7133+153del
XM_017009971.2:c.7133+152_7133+153del XP_016865460.1:n.7133+152_7133+153del
XM_017009972.1:c.251+152_251+153del XP_016865461.1:n.251+152_251+153del
XM_017009973.1:c.251+152_251+153del XP_016865462.1:n.251+152_251+153del
XM_017009974.2:c.7133+152_7133+153del XP_016865463.1:n.7133+152_7133+153del
NR_003149.2:n.7149+152_7149+153del