Canonical Allele Identifier: CA182163
Gene: ADGRV1 HGNC NCBI

Linked Data

ClinVar Variation Id: 178354
dbSNP Id: rs200197273
gnomAD v2: 5-89923208-C-G
gnomAD v3: 5-90627391-C-G
gnomAD v4: 5-90627391-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627391C>G , CM000667.2:g.90627391C>G GRCh38
NC_000005.9:g.89923208C>G , CM000667.1:g.89923208C>G GRCh37
NC_000005.8:g.89958964C>G NCBI36
NG_007083.1:g.73592C>G
NG_007083.2:g.103048C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.853C>G MANE Select ENSP00000384582.2:p.Arg285Gly
ENST00000640083.1:n.558C>G
ENST00000640109.1:n.949C>G
ENST00000640281.1:n.912C>G
ENST00000405460.6:c.853C>G ENSP00000384582.2:p.Arg285Gly
NM_032119.3:c.853C>G NP_115495.3:p.Arg285Gly
NR_003149.1:n.949C>G
XM_011543675.1:c.853C>G XP_011541977.1:p.Arg285Gly
XM_011543676.1:c.853C>G XP_011541978.1:p.Arg285Gly
XM_011543678.1:c.853C>G XP_011541980.1:p.Arg285Gly
XM_011543679.1:c.853C>G XP_011541981.1:p.Arg285Gly
NM_032119.4:c.853C>G MANE Select NP_115495.3:p.Arg285Gly
XM_017009963.2:c.853C>G XP_016865452.1:p.Arg285Gly
XM_017009964.2:c.853C>G XP_016865453.1:p.Arg285Gly
XM_017009965.1:c.850C>G XP_016865454.1:p.Arg284Gly
XM_017009966.2:c.853C>G XP_016865455.1:p.Arg285Gly
XM_017009967.1:c.757C>G XP_016865456.1:p.Arg253Gly
XM_017009968.2:c.853C>G XP_016865457.1:p.Arg285Gly
XM_017009969.2:c.853C>G XP_016865458.1:p.Arg285Gly
XM_017009970.2:c.853C>G XP_016865459.1:p.Arg285Gly
XM_017009971.2:c.853C>G XP_016865460.1:p.Arg285Gly
XM_017009974.2:c.853C>G XP_016865463.1:p.Arg285Gly
NR_003149.2:n.952C>G