Canonical Allele Identifier: CA3339659
Community Standard Title: NM_032119.4(ADGRV1):c.5782A>C (p.Ser1928Arg)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90683703A>C , CM000667.2:g.90683703A>C GRCh38
NC_000005.9:g.89979520A>C , CM000667.1:g.89979520A>C GRCh37
NC_000005.8:g.90015276A>C NCBI36
NG_007083.1:g.129904A>C
NG_007083.2:g.159360A>C

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.5782A>C MANE Select NP_115495.3:p.Ser1928Arg
ENST00000405460.9:c.5782A>C MANE Select ENSP00000384582.2:p.Ser1928Arg
NM_032119.3:c.5782A>C NP_115495.3:p.Ser1928Arg
NR_003149.1:n.5878A>C
NR_003149.2:n.5881A>C
ENST00000405460.6:c.5782A>C ENSP00000384582.2:p.Ser1928Arg
ENST00000639431.1:c.265+7494A>C ENSP00000491057.1:n.265+7494A>C
ENST00000639473.1:n.1241A>C
ENST00000640012.1:c.165-2077A>C
ENST00000640403.1:c.3073A>C ENSP00000492531.1:p.Ser1025Arg
ENST00000640779.1:c.594A>C
XM_011543675.1:c.5779A>C XP_011541977.1:p.Ser1927Arg
XM_011543676.1:c.5701A>C XP_011541978.1:p.Ser1901Arg
XM_011543677.1:c.3085A>C XP_011541979.1:p.Ser1029Arg
XM_011543678.1:c.5782A>C XP_011541980.1:p.Ser1928Arg
XM_011543679.1:c.5782A>C XP_011541981.1:p.Ser1928Arg
XM_017009963.2:c.5782A>C XP_016865452.1:p.Ser1928Arg
XM_017009964.2:c.5779A>C XP_016865453.1:p.Ser1927Arg
XM_017009965.1:c.5779A>C XP_016865454.1:p.Ser1927Arg
XM_017009966.2:c.5701A>C XP_016865455.1:p.Ser1901Arg
XM_017009967.1:c.5686A>C XP_016865456.1:p.Ser1896Arg
XM_017009968.2:c.5782A>C XP_016865457.1:p.Ser1928Arg
XM_017009969.2:c.5782A>C XP_016865458.1:p.Ser1928Arg
XM_017009970.2:c.5782A>C XP_016865459.1:p.Ser1928Arg
XM_017009971.2:c.5782A>C XP_016865460.1:p.Ser1928Arg
XM_017009973.1:c.-1018A>C XP_016865462.1:n.-1018A>C
XM_017009974.2:c.5782A>C XP_016865463.1:p.Ser1928Arg