Canonical Allele Identifier: CA1562836896
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90644769G= , CM000667.2:g.90644769G= GRCh38
NC_000005.9:g.89940586G= , CM000667.1:g.89940586G= GRCh37
NC_000005.8:g.89976342G= NCBI36
NG_007083.1:g.90970G=
NG_007083.2:g.120426G=

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.2798G= MANE Select ENSP00000384582.2:p.Ser933=
ENST00000504142.2:n.1564G=
ENST00000639676.1:n.396G=
ENST00000640403.1:c.101G= ENSP00000492531.1:p.Ser34=
ENST00000405460.6:c.2798G= ENSP00000384582.2:p.Ser933=
ENST00000504142.1:c.1563G=
NM_032119.3:c.2798G= NP_115495.3:p.Ser933=
NR_003149.1:n.2894G=
XM_011543675.1:c.2798G= XP_011541977.1:p.Ser933=
XM_011543676.1:c.2798G= XP_011541978.1:p.Ser933=
XM_011543677.1:c.101G= XP_011541979.1:p.Ser34=
XM_011543678.1:c.2798G= XP_011541980.1:p.Ser933=
XM_011543679.1:c.2798G= XP_011541981.1:p.Ser933=
NM_032119.4:c.2798G= MANE Select NP_115495.3:p.Ser933=
XM_017009963.2:c.2798G= XP_016865452.1:p.Ser933=
XM_017009964.2:c.2798G= XP_016865453.1:p.Ser933=
XM_017009965.1:c.2795G= XP_016865454.1:p.Ser932=
XM_017009966.2:c.2798G= XP_016865455.1:p.Ser933=
XM_017009967.1:c.2702G= XP_016865456.1:p.Ser901=
XM_017009968.2:c.2798G= XP_016865457.1:p.Ser933=
XM_017009969.2:c.2798G= XP_016865458.1:p.Ser933=
XM_017009970.2:c.2798G= XP_016865459.1:p.Ser933=
XM_017009971.2:c.2798G= XP_016865460.1:p.Ser933=
XM_017009974.2:c.2798G= XP_016865463.1:p.Ser933=
NR_003149.2:n.2897G=