Canonical Allele Identifier: CA3340929
Community Standard Title: NM_032119.4(ADGRV1):c.11222G>A (p.Arg3741His)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90753674G>A , CM000667.2:g.90753674G>A GRCh38
NC_000005.9:g.90049491G>A , CM000667.1:g.90049491G>A GRCh37
NC_000005.8:g.90085247G>A NCBI36
NG_007083.1:g.199875G>A
NG_007083.2:g.229331G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.11222G>A MANE Select NP_115495.3:p.Arg3741His
ENST00000405460.9:c.11222G>A MANE Select ENSP00000384582.2:p.Arg3741His
NM_032119.3:c.11222G>A NP_115495.3:p.Arg3741His
NR_003149.1:n.11235G>A
NR_003149.2:n.11238G>A
ENST00000405460.6:c.11222G>A ENSP00000384582.2:p.Arg3741His
ENST00000425867.3:c.353G>A ENSP00000392618.3:p.Arg118His
ENST00000509621.1:c.3919G>A
ENST00000639431.1:c.265+77465G>A ENSP00000491057.1:n.265+77465G>A
ENST00000640374.1:n.4366G>A
ENST00000640464.1:n.1641G>A
XM_011543675.1:c.11219G>A XP_011541977.1:p.Arg3740His
XM_011543676.1:c.11141G>A XP_011541978.1:p.Arg3714His
XM_011543677.1:c.8525G>A XP_011541979.1:p.Arg2842His
XM_011543678.1:c.11222G>A XP_011541980.1:p.Arg3741His
XM_017009963.2:c.11243G>A XP_016865452.1:p.Arg3748His
XM_017009964.2:c.11240G>A XP_016865453.1:p.Arg3747His
XM_017009965.1:c.11240G>A XP_016865454.1:p.Arg3747His
XM_017009966.2:c.11162G>A XP_016865455.1:p.Arg3721His
XM_017009967.1:c.11147G>A XP_016865456.1:p.Arg3716His
XM_017009968.2:c.11243G>A XP_016865457.1:p.Arg3748His
XM_017009969.2:c.11243G>A XP_016865458.1:p.Arg3748His
XM_017009970.2:c.11243G>A XP_016865459.1:p.Arg3748His
XM_017009971.2:c.11243G>A XP_016865460.1:p.Arg3748His
XM_017009972.1:c.4361G>A XP_016865461.1:p.Arg1454His
XM_017009973.1:c.4340G>A XP_016865462.1:p.Arg1447His