Canonical Allele Identifier: CA2767420648
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692914_90692919del , CM000667.2:g.90692914_90692919del GRCh38
NC_000005.9:g.89988731_89988736del , CM000667.1:g.89988731_89988736del GRCh37
NC_000005.8:g.90024487_90024492del NCBI36
NG_007083.1:g.139115_139120del
NG_007083.2:g.168571_168576del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7133+128_7133+133del MANE Select ENSP00000384582.2:n.7133+128_7133+133del
ENST00000639431.1:c.265+16705_265+16710del ENSP00000491057.1:n.265+16705_265+16710del
ENST00000639473.1:n.2592+128_2592+133del
ENST00000640012.1:c.940+128_940+133del
ENST00000640374.1:n.277+128_277+133del
ENST00000640403.1:c.4424+128_4424+133del ENSP00000492531.1:n.4424+128_4424+133del
ENST00000640779.1:c.1862+128_1862+133del
ENST00000405460.6:c.7133+128_7133+133del ENSP00000384582.2:n.7133+128_7133+133del
NM_032119.3:c.7133+128_7133+133del NP_115495.3:n.7133+128_7133+133del
NR_003149.1:n.7146+128_7146+133del
XM_011543675.1:c.7130+128_7130+133del XP_011541977.1:n.7130+128_7130+133del
XM_011543676.1:c.7052+128_7052+133del XP_011541978.1:n.7052+128_7052+133del
XM_011543677.1:c.4436+128_4436+133del XP_011541979.1:n.4436+128_4436+133del
XM_011543678.1:c.7133+128_7133+133del XP_011541980.1:n.7133+128_7133+133del
XM_011543679.1:c.7133+128_7133+133del XP_011541981.1:n.7133+128_7133+133del
NM_032119.4:c.7133+128_7133+133del MANE Select NP_115495.3:n.7133+128_7133+133del
XM_017009963.2:c.7133+128_7133+133del XP_016865452.1:n.7133+128_7133+133del
XM_017009964.2:c.7130+128_7130+133del XP_016865453.1:n.7130+128_7130+133del
XM_017009965.1:c.7130+128_7130+133del XP_016865454.1:n.7130+128_7130+133del
XM_017009966.2:c.7052+128_7052+133del XP_016865455.1:n.7052+128_7052+133del
XM_017009967.1:c.7037+128_7037+133del XP_016865456.1:n.7037+128_7037+133del
XM_017009968.2:c.7133+128_7133+133del XP_016865457.1:n.7133+128_7133+133del
XM_017009969.2:c.7133+128_7133+133del XP_016865458.1:n.7133+128_7133+133del
XM_017009970.2:c.7133+128_7133+133del XP_016865459.1:n.7133+128_7133+133del
XM_017009971.2:c.7133+128_7133+133del XP_016865460.1:n.7133+128_7133+133del
XM_017009972.1:c.251+128_251+133del XP_016865461.1:n.251+128_251+133del
XM_017009973.1:c.251+128_251+133del XP_016865462.1:n.251+128_251+133del
XM_017009974.2:c.7133+128_7133+133del XP_016865463.1:n.7133+128_7133+133del
NR_003149.2:n.7149+128_7149+133del