Canonical Allele Identifier: CA360403208
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90725571A>G , CM000667.2:g.90725571A>G GRCh38
NC_000005.9:g.90021388A>G , CM000667.1:g.90021388A>G GRCh37
NC_000005.8:g.90057144A>G NCBI36
NG_007083.1:g.171772A>G
NG_007083.2:g.201228A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.10076A>G MANE Select ENSP00000384582.2:p.Glu3359Gly
ENST00000639431.1:c.265+49362A>G ENSP00000491057.1:n.265+49362A>G
ENST00000640374.1:n.3220A>G
ENST00000640464.1:n.495A>G
ENST00000405460.6:c.10076A>G ENSP00000384582.2:p.Glu3359Gly
ENST00000509621.1:c.2773A>G
NM_032119.3:c.10076A>G NP_115495.3:p.Glu3359Gly
NR_003149.1:n.10089A>G
XM_011543675.1:c.10073A>G XP_011541977.1:p.Glu3358Gly
XM_011543676.1:c.9995A>G XP_011541978.1:p.Glu3332Gly
XM_011543677.1:c.7379A>G XP_011541979.1:p.Glu2460Gly
XM_011543678.1:c.10076A>G XP_011541980.1:p.Glu3359Gly
XM_011543679.1:c.10076A>G XP_011541981.1:p.Glu3359Gly
XR_948560.1:n.272-9762T>C
NM_032119.4:c.10076A>G MANE Select NP_115495.3:p.Glu3359Gly
XM_017009963.2:c.10097A>G XP_016865452.1:p.Glu3366Gly
XM_017009964.2:c.10094A>G XP_016865453.1:p.Glu3365Gly
XM_017009965.1:c.10094A>G XP_016865454.1:p.Glu3365Gly
XM_017009966.2:c.10016A>G XP_016865455.1:p.Glu3339Gly
XM_017009967.1:c.10001A>G XP_016865456.1:p.Glu3334Gly
XM_017009968.2:c.10097A>G XP_016865457.1:p.Glu3366Gly
XM_017009969.2:c.10097A>G XP_016865458.1:p.Glu3366Gly
XM_017009970.2:c.10097A>G XP_016865459.1:p.Glu3366Gly
XM_017009971.2:c.10097A>G XP_016865460.1:p.Glu3366Gly
XM_017009972.1:c.3215A>G XP_016865461.1:p.Glu1072Gly
XM_017009973.1:c.3194A>G XP_016865462.1:p.Glu1065Gly
XM_017009974.2:c.10097A>G XP_016865463.1:p.Glu3366Gly
XR_001742802.1:n.2523-9762T>C
NR_003149.2:n.10092A>G