Canonical Allele Identifier: CA360414273
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90684088C>G , CM000667.2:g.90684088C>G GRCh38
NC_000005.9:g.89979905C>G , CM000667.1:g.89979905C>G GRCh37
NC_000005.8:g.90015661C>G NCBI36
NG_007083.1:g.130289C>G
NG_007083.2:g.159745C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.6167C>G MANE Select ENSP00000384582.2:p.Ala2056Gly
ENST00000639431.1:c.265+7879C>G ENSP00000491057.1:n.265+7879C>G
ENST00000639473.1:n.1626C>G
ENST00000640012.1:c.165-1692C>G
ENST00000640403.1:c.3458C>G ENSP00000492531.1:p.Ala1153Gly
ENST00000640779.1:c.979C>G
ENST00000405460.6:c.6167C>G ENSP00000384582.2:p.Ala2056Gly
NM_032119.3:c.6167C>G NP_115495.3:p.Ala2056Gly
NR_003149.1:n.6263C>G
XM_011543675.1:c.6164C>G XP_011541977.1:p.Ala2055Gly
XM_011543676.1:c.6086C>G XP_011541978.1:p.Ala2029Gly
XM_011543677.1:c.3470C>G XP_011541979.1:p.Ala1157Gly
XM_011543678.1:c.6167C>G XP_011541980.1:p.Ala2056Gly
XM_011543679.1:c.6167C>G XP_011541981.1:p.Ala2056Gly
NM_032119.4:c.6167C>G MANE Select NP_115495.3:p.Ala2056Gly
XM_017009963.2:c.6167C>G XP_016865452.1:p.Ala2056Gly
XM_017009964.2:c.6164C>G XP_016865453.1:p.Ala2055Gly
XM_017009965.1:c.6164C>G XP_016865454.1:p.Ala2055Gly
XM_017009966.2:c.6086C>G XP_016865455.1:p.Ala2029Gly
XM_017009967.1:c.6071C>G XP_016865456.1:p.Ala2024Gly
XM_017009968.2:c.6167C>G XP_016865457.1:p.Ala2056Gly
XM_017009969.2:c.6167C>G XP_016865458.1:p.Ala2056Gly
XM_017009970.2:c.6167C>G XP_016865459.1:p.Ala2056Gly
XM_017009971.2:c.6167C>G XP_016865460.1:p.Ala2056Gly
XM_017009973.1:c.-633C>G XP_016865462.1:n.-633C>G
XM_017009974.2:c.6167C>G XP_016865463.1:p.Ala2056Gly
NR_003149.2:n.6266C>G