Canonical Allele Identifier: CA2674568740
Gene: ADGRV1 HGNC NCBI

Linked Data

gnomAD v4: 5-90703574-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90703574A>G , CM000667.2:g.90703574A>G GRCh38
NC_000005.9:g.89999391A>G , CM000667.1:g.89999391A>G GRCh37
NC_000005.8:g.90035147A>G NCBI36
NG_007083.1:g.149775A>G
NG_007083.2:g.179231A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.8156-91A>G MANE Select ENSP00000384582.2:n.8156-91A>G
ENST00000639431.1:c.265+27365A>G ENSP00000491057.1:n.265+27365A>G
ENST00000639473.1:n.3615-91A>G
ENST00000640012.1:c.1963-91A>G
ENST00000640374.1:n.1300-91A>G
ENST00000640403.1:c.5447-91A>G ENSP00000492531.1:n.5447-91A>G
ENST00000640779.1:c.2885-91A>G
ENST00000405460.6:c.8156-91A>G ENSP00000384582.2:n.8156-91A>G
ENST00000509621.1:c.853-91A>G
NM_032119.3:c.8156-91A>G NP_115495.3:n.8156-91A>G
NR_003149.1:n.8169-91A>G
XM_011543675.1:c.8153-91A>G XP_011541977.1:n.8153-91A>G
XM_011543676.1:c.8075-91A>G XP_011541978.1:n.8075-91A>G
XM_011543677.1:c.5459-91A>G XP_011541979.1:n.5459-91A>G
XM_011543678.1:c.8156-91A>G XP_011541980.1:n.8156-91A>G
XM_011543679.1:c.8156-91A>G XP_011541981.1:n.8156-91A>G
NM_032119.4:c.8156-91A>G MANE Select NP_115495.3:n.8156-91A>G
XM_017009963.2:c.8156-91A>G XP_016865452.1:n.8156-91A>G
XM_017009964.2:c.8153-91A>G XP_016865453.1:n.8153-91A>G
XM_017009965.1:c.8153-91A>G XP_016865454.1:n.8153-91A>G
XM_017009966.2:c.8075-91A>G XP_016865455.1:n.8075-91A>G
XM_017009967.1:c.8060-91A>G XP_016865456.1:n.8060-91A>G
XM_017009968.2:c.8156-91A>G XP_016865457.1:n.8156-91A>G
XM_017009969.2:c.8156-91A>G XP_016865458.1:n.8156-91A>G
XM_017009970.2:c.8156-91A>G XP_016865459.1:n.8156-91A>G
XM_017009971.2:c.8156-91A>G XP_016865460.1:n.8156-91A>G
XM_017009972.1:c.1274-91A>G XP_016865461.1:n.1274-91A>G
XM_017009973.1:c.1274-91A>G XP_016865462.1:n.1274-91A>G
XM_017009974.2:c.8156-91A>G XP_016865463.1:n.8156-91A>G
NR_003149.2:n.8172-91A>G