Canonical Allele Identifier: CA2767420631
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692893_90692899del , CM000667.2:g.90692893_90692899del GRCh38
NC_000005.9:g.89988710_89988716del , CM000667.1:g.89988710_89988716del GRCh37
NC_000005.8:g.90024466_90024472del NCBI36
NG_007083.1:g.139094_139100del
NG_007083.2:g.168550_168556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7133+107_7133+113del MANE Select ENSP00000384582.2:n.7133+107_7133+113del
ENST00000639431.1:c.265+16684_265+16690del ENSP00000491057.1:n.265+16684_265+16690del
ENST00000639473.1:n.2592+107_2592+113del
ENST00000640012.1:c.940+107_940+113del
ENST00000640374.1:n.277+107_277+113del
ENST00000640403.1:c.4424+107_4424+113del ENSP00000492531.1:n.4424+107_4424+113del
ENST00000640779.1:c.1862+107_1862+113del
ENST00000405460.6:c.7133+107_7133+113del ENSP00000384582.2:n.7133+107_7133+113del
NM_032119.3:c.7133+107_7133+113del NP_115495.3:n.7133+107_7133+113del
NR_003149.1:n.7146+107_7146+113del
XM_011543675.1:c.7130+107_7130+113del XP_011541977.1:n.7130+107_7130+113del
XM_011543676.1:c.7052+107_7052+113del XP_011541978.1:n.7052+107_7052+113del
XM_011543677.1:c.4436+107_4436+113del XP_011541979.1:n.4436+107_4436+113del
XM_011543678.1:c.7133+107_7133+113del XP_011541980.1:n.7133+107_7133+113del
XM_011543679.1:c.7133+107_7133+113del XP_011541981.1:n.7133+107_7133+113del
NM_032119.4:c.7133+107_7133+113del MANE Select NP_115495.3:n.7133+107_7133+113del
XM_017009963.2:c.7133+107_7133+113del XP_016865452.1:n.7133+107_7133+113del
XM_017009964.2:c.7130+107_7130+113del XP_016865453.1:n.7130+107_7130+113del
XM_017009965.1:c.7130+107_7130+113del XP_016865454.1:n.7130+107_7130+113del
XM_017009966.2:c.7052+107_7052+113del XP_016865455.1:n.7052+107_7052+113del
XM_017009967.1:c.7037+107_7037+113del XP_016865456.1:n.7037+107_7037+113del
XM_017009968.2:c.7133+107_7133+113del XP_016865457.1:n.7133+107_7133+113del
XM_017009969.2:c.7133+107_7133+113del XP_016865458.1:n.7133+107_7133+113del
XM_017009970.2:c.7133+107_7133+113del XP_016865459.1:n.7133+107_7133+113del
XM_017009971.2:c.7133+107_7133+113del XP_016865460.1:n.7133+107_7133+113del
XM_017009972.1:c.251+107_251+113del XP_016865461.1:n.251+107_251+113del
XM_017009973.1:c.251+107_251+113del XP_016865462.1:n.251+107_251+113del
XM_017009974.2:c.7133+107_7133+113del XP_016865463.1:n.7133+107_7133+113del
NR_003149.2:n.7149+107_7149+113del