Canonical Allele Identifier: CA2767420603
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692862_90692863del , CM000667.2:g.90692862_90692863del GRCh38
NC_000005.9:g.89988679_89988680del , CM000667.1:g.89988679_89988680del GRCh37
NC_000005.8:g.90024435_90024436del NCBI36
NG_007083.1:g.139063_139064del
NG_007083.2:g.168519_168520del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7133+76_7133+77del MANE Select ENSP00000384582.2:n.7133+76_7133+77del
ENST00000639431.1:c.265+16653_265+16654del ENSP00000491057.1:n.265+16653_265+16654del
ENST00000639473.1:n.2592+76_2592+77del
ENST00000640012.1:c.940+76_940+77del
ENST00000640374.1:n.277+76_277+77del
ENST00000640403.1:c.4424+76_4424+77del ENSP00000492531.1:n.4424+76_4424+77del
ENST00000640779.1:c.1862+76_1862+77del
ENST00000405460.6:c.7133+76_7133+77del ENSP00000384582.2:n.7133+76_7133+77del
NM_032119.3:c.7133+76_7133+77del NP_115495.3:n.7133+76_7133+77del
NR_003149.1:n.7146+76_7146+77del
XM_011543675.1:c.7130+76_7130+77del XP_011541977.1:n.7130+76_7130+77del
XM_011543676.1:c.7052+76_7052+77del XP_011541978.1:n.7052+76_7052+77del
XM_011543677.1:c.4436+76_4436+77del XP_011541979.1:n.4436+76_4436+77del
XM_011543678.1:c.7133+76_7133+77del XP_011541980.1:n.7133+76_7133+77del
XM_011543679.1:c.7133+76_7133+77del XP_011541981.1:n.7133+76_7133+77del
NM_032119.4:c.7133+76_7133+77del MANE Select NP_115495.3:n.7133+76_7133+77del
XM_017009963.2:c.7133+76_7133+77del XP_016865452.1:n.7133+76_7133+77del
XM_017009964.2:c.7130+76_7130+77del XP_016865453.1:n.7130+76_7130+77del
XM_017009965.1:c.7130+76_7130+77del XP_016865454.1:n.7130+76_7130+77del
XM_017009966.2:c.7052+76_7052+77del XP_016865455.1:n.7052+76_7052+77del
XM_017009967.1:c.7037+76_7037+77del XP_016865456.1:n.7037+76_7037+77del
XM_017009968.2:c.7133+76_7133+77del XP_016865457.1:n.7133+76_7133+77del
XM_017009969.2:c.7133+76_7133+77del XP_016865458.1:n.7133+76_7133+77del
XM_017009970.2:c.7133+76_7133+77del XP_016865459.1:n.7133+76_7133+77del
XM_017009971.2:c.7133+76_7133+77del XP_016865460.1:n.7133+76_7133+77del
XM_017009972.1:c.251+76_251+77del XP_016865461.1:n.251+76_251+77del
XM_017009973.1:c.251+76_251+77del XP_016865462.1:n.251+76_251+77del
XM_017009974.2:c.7133+76_7133+77del XP_016865463.1:n.7133+76_7133+77del
NR_003149.2:n.7149+76_7149+77del