Canonical Allele Identifier: CA360367065
Gene: ADGRV1 HGNC NCBI

Linked Data

gnomAD v4: 5-90755123-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90755123G>A , CM000667.2:g.90755123G>A GRCh38
NC_000005.9:g.90050940G>A , CM000667.1:g.90050940G>A GRCh37
NC_000005.8:g.90086696G>A NCBI36
NG_007083.1:g.201324G>A
NG_007083.2:g.230780G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.11518G>A MANE Select ENSP00000384582.2:p.Glu3840Lys
ENST00000425867.3:c.649G>A ENSP00000392618.3:p.Glu217Lys
ENST00000639431.1:c.265+78914G>A ENSP00000491057.1:n.265+78914G>A
ENST00000640374.1:n.4662G>A
ENST00000640464.1:n.1937G>A
ENST00000405460.6:c.11518G>A ENSP00000384582.2:p.Glu3840Lys
ENST00000509621.1:c.4215G>A
NM_032119.3:c.11518G>A NP_115495.3:p.Glu3840Lys
NR_003149.1:n.11531G>A
XM_011543675.1:c.11515G>A XP_011541977.1:p.Glu3839Lys
XM_011543676.1:c.11437G>A XP_011541978.1:p.Glu3813Lys
XM_011543677.1:c.8821G>A XP_011541979.1:p.Glu2941Lys
XM_011543678.1:c.11518G>A XP_011541980.1:p.Glu3840Lys
NM_032119.4:c.11518G>A MANE Select NP_115495.3:p.Glu3840Lys
XM_017009963.2:c.11539G>A XP_016865452.1:p.Glu3847Lys
XM_017009964.2:c.11536G>A XP_016865453.1:p.Glu3846Lys
XM_017009965.1:c.11536G>A XP_016865454.1:p.Glu3846Lys
XM_017009966.2:c.11458G>A XP_016865455.1:p.Glu3820Lys
XM_017009967.1:c.11443G>A XP_016865456.1:p.Glu3815Lys
XM_017009968.2:c.11539G>A XP_016865457.1:p.Glu3847Lys
XM_017009969.2:c.11539G>A XP_016865458.1:p.Glu3847Lys
XM_017009970.2:c.11539G>A XP_016865459.1:p.Glu3847Lys
XM_017009971.2:c.11539G>A XP_016865460.1:p.Glu3847Lys
XM_017009972.1:c.4657G>A XP_016865461.1:p.Glu1553Lys
XM_017009973.1:c.4636G>A XP_016865462.1:p.Glu1546Lys
NR_003149.2:n.11534G>A