Canonical Allele Identifier: CA360413377
Community Standard Title: NM_032119.4(ADGRV1):c.5784C>A (p.Ser1928Arg)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90683705C>A , CM000667.2:g.90683705C>A GRCh38
NC_000005.9:g.89979522C>A , CM000667.1:g.89979522C>A GRCh37
NC_000005.8:g.90015278C>A NCBI36
NG_007083.1:g.129906C>A
NG_007083.2:g.159362C>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.5784C>A MANE Select NP_115495.3:p.Ser1928Arg
ENST00000405460.9:c.5784C>A MANE Select ENSP00000384582.2:p.Ser1928Arg
NM_032119.3:c.5784C>A NP_115495.3:p.Ser1928Arg
NR_003149.1:n.5880C>A
NR_003149.2:n.5883C>A
ENST00000405460.6:c.5784C>A ENSP00000384582.2:p.Ser1928Arg
ENST00000639431.1:c.265+7496C>A ENSP00000491057.1:n.265+7496C>A
ENST00000639473.1:n.1243C>A
ENST00000640012.1:c.165-2075C>A
ENST00000640403.1:c.3075C>A ENSP00000492531.1:p.Ser1025Arg
ENST00000640779.1:c.596C>A
XM_011543675.1:c.5781C>A XP_011541977.1:p.Ser1927Arg
XM_011543676.1:c.5703C>A XP_011541978.1:p.Ser1901Arg
XM_011543677.1:c.3087C>A XP_011541979.1:p.Ser1029Arg
XM_011543678.1:c.5784C>A XP_011541980.1:p.Ser1928Arg
XM_011543679.1:c.5784C>A XP_011541981.1:p.Ser1928Arg
XM_017009963.2:c.5784C>A XP_016865452.1:p.Ser1928Arg
XM_017009964.2:c.5781C>A XP_016865453.1:p.Ser1927Arg
XM_017009965.1:c.5781C>A XP_016865454.1:p.Ser1927Arg
XM_017009966.2:c.5703C>A XP_016865455.1:p.Ser1901Arg
XM_017009967.1:c.5688C>A XP_016865456.1:p.Ser1896Arg
XM_017009968.2:c.5784C>A XP_016865457.1:p.Ser1928Arg
XM_017009969.2:c.5784C>A XP_016865458.1:p.Ser1928Arg
XM_017009970.2:c.5784C>A XP_016865459.1:p.Ser1928Arg
XM_017009971.2:c.5784C>A XP_016865460.1:p.Ser1928Arg
XM_017009973.1:c.-1016C>A XP_016865462.1:n.-1016C>A
XM_017009974.2:c.5784C>A XP_016865463.1:p.Ser1928Arg