Canonical Allele Identifier: CA360366990
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627484G>A , CM000667.2:g.90627484G>A GRCh38
NC_000005.9:g.89923301G>A , CM000667.1:g.89923301G>A GRCh37
NC_000005.8:g.89959057G>A NCBI36
NG_007083.1:g.73685G>A
NG_007083.2:g.103141G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.946G>A MANE Select ENSP00000384582.2:p.Ala316Thr
ENST00000640083.1:n.651G>A
ENST00000640109.1:n.1042G>A
ENST00000640281.1:n.1005G>A
ENST00000405460.6:c.946G>A ENSP00000384582.2:p.Ala316Thr
NM_032119.3:c.946G>A NP_115495.3:p.Ala316Thr
NR_003149.1:n.1042G>A
XM_011543675.1:c.946G>A XP_011541977.1:p.Ala316Thr
XM_011543676.1:c.946G>A XP_011541978.1:p.Ala316Thr
XM_011543678.1:c.946G>A XP_011541980.1:p.Ala316Thr
XM_011543679.1:c.946G>A XP_011541981.1:p.Ala316Thr
NM_032119.4:c.946G>A MANE Select NP_115495.3:p.Ala316Thr
XM_017009963.2:c.946G>A XP_016865452.1:p.Ala316Thr
XM_017009964.2:c.946G>A XP_016865453.1:p.Ala316Thr
XM_017009965.1:c.943G>A XP_016865454.1:p.Ala315Thr
XM_017009966.2:c.946G>A XP_016865455.1:p.Ala316Thr
XM_017009967.1:c.850G>A XP_016865456.1:p.Ala284Thr
XM_017009968.2:c.946G>A XP_016865457.1:p.Ala316Thr
XM_017009969.2:c.946G>A XP_016865458.1:p.Ala316Thr
XM_017009970.2:c.946G>A XP_016865459.1:p.Ala316Thr
XM_017009971.2:c.946G>A XP_016865460.1:p.Ala316Thr
XM_017009974.2:c.946G>A XP_016865463.1:p.Ala316Thr
NR_003149.2:n.1045G>A