Canonical Allele Identifier: CA360410307
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90675427C>A , CM000667.2:g.90675427C>A GRCh38
NC_000005.9:g.89971244C>A , CM000667.1:g.89971244C>A GRCh37
NC_000005.8:g.90007000C>A NCBI36
NG_007083.1:g.121628C>A
NG_007083.2:g.151084C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.5295C>A MANE Select ENSP00000384582.2:p.Phe1765Leu
ENST00000639431.1:c.117C>A ENSP00000491057.1:p.Phe39Leu
ENST00000639473.1:n.754C>A
ENST00000640403.1:c.2586C>A ENSP00000492531.1:p.Phe862Leu
ENST00000640779.1:c.110C>A
ENST00000405460.6:c.5295C>A ENSP00000384582.2:p.Phe1765Leu
ENST00000450321.2:n.630C>A
NM_032119.3:c.5295C>A NP_115495.3:p.Phe1765Leu
NR_003149.1:n.5391C>A
XM_011543675.1:c.5295C>A XP_011541977.1:p.Phe1765Leu
XM_011543676.1:c.5295C>A XP_011541978.1:p.Phe1765Leu
XM_011543677.1:c.2598C>A XP_011541979.1:p.Phe866Leu
XM_011543678.1:c.5295C>A XP_011541980.1:p.Phe1765Leu
XM_011543679.1:c.5295C>A XP_011541981.1:p.Phe1765Leu
NM_032119.4:c.5295C>A MANE Select NP_115495.3:p.Phe1765Leu
XM_017009963.2:c.5295C>A XP_016865452.1:p.Phe1765Leu
XM_017009964.2:c.5295C>A XP_016865453.1:p.Phe1765Leu
XM_017009965.1:c.5292C>A XP_016865454.1:p.Phe1764Leu
XM_017009966.2:c.5295C>A XP_016865455.1:p.Phe1765Leu
XM_017009967.1:c.5199C>A XP_016865456.1:p.Phe1733Leu
XM_017009968.2:c.5295C>A XP_016865457.1:p.Phe1765Leu
XM_017009969.2:c.5295C>A XP_016865458.1:p.Phe1765Leu
XM_017009970.2:c.5295C>A XP_016865459.1:p.Phe1765Leu
XM_017009971.2:c.5295C>A XP_016865460.1:p.Phe1765Leu
XM_017009973.1:c.-1502C>A XP_016865462.1:n.-1502C>A
XM_017009974.2:c.5295C>A XP_016865463.1:p.Phe1765Leu
NR_003149.2:n.5394C>A