Canonical Allele Identifier: CA122805777
Community Standard Title: NM_032119.4(ADGRV1):c.16573G>A (p.Gly5525Arg)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90829148G>A , CM000667.2:g.90829148G>A GRCh38
NC_000005.9:g.90124965G>A , CM000667.1:g.90124965G>A GRCh37
NC_000005.8:g.90160721G>A NCBI36
NG_007083.1:g.275349G>A
NG_007083.2:g.304805G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.16573G>A MANE Select NP_115495.3:p.Gly5525Arg
ENST00000405460.9:c.16573G>A MANE Select ENSP00000384582.2:p.Gly5525Arg
NM_032119.3:c.16573G>A NP_115495.3:p.Gly5525Arg
NR_003149.1:n.16586G>A
NR_003149.2:n.16589G>A
ENST00000405460.6:c.16573G>A ENSP00000384582.2:p.Gly5525Arg
ENST00000425867.2:c.3556G>A ENSP00000392618.2:p.Gly1186Arg
ENST00000425867.3:c.5527G>A ENSP00000392618.3:p.Gly1843Arg
ENST00000638510.1:n.3840G>A
ENST00000639431.1:c.265+152939G>A ENSP00000491057.1:n.265+152939G>A
ENST00000640061.1:n.128+6966G>A
ENST00000640407.1:c.3022G>A ENSP00000491425.1:n.3022G>A
XM_011543675.1:c.16570G>A XP_011541977.1:p.Gly5524Arg
XM_011543676.1:c.16492G>A XP_011541978.1:p.Gly5498Arg
XM_011543677.1:c.13876G>A XP_011541979.1:p.Gly4626Arg
XM_017009963.2:c.16594G>A XP_016865452.1:p.Gly5532Arg
XM_017009964.2:c.16591G>A XP_016865453.1:p.Gly5531Arg
XM_017009965.1:c.16591G>A XP_016865454.1:p.Gly5531Arg
XM_017009966.2:c.16513G>A XP_016865455.1:p.Gly5505Arg
XM_017009967.1:c.16498G>A XP_016865456.1:p.Gly5500Arg
XM_017009968.2:c.16414G>A XP_016865457.1:p.Gly5472Arg
XM_017009969.2:c.16594G>A XP_016865458.1:p.Gly5532Arg
XM_017009972.1:c.9712G>A XP_016865461.1:p.Gly3238Arg
XM_017009973.1:c.9691G>A XP_016865462.1:p.Gly3231Arg