Canonical Allele Identifier: CA121839869
Community Standard Title: NM_032119.4(ADGRV1):c.4080G>A (p.Trp1360Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90653654G>A , CM000667.2:g.90653654G>A GRCh38
NC_000005.9:g.89949471G>A , CM000667.1:g.89949471G>A GRCh37
NC_000005.8:g.89985227G>A NCBI36
NG_007083.1:g.99855G>A
NG_007083.2:g.129311G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.4080G>A MANE Select NP_115495.3:p.Trp1360Ter
ENST00000405460.9:c.4080G>A MANE Select ENSP00000384582.2:p.Trp1360Ter
NM_032119.3:c.4080G>A NP_115495.3:p.Trp1360Ter
NR_003149.1:n.4176G>A
NR_003149.2:n.4179G>A
ENST00000405460.6:c.4080G>A ENSP00000384582.2:p.Trp1360Ter
ENST00000504142.1:c.2845G>A
ENST00000504142.2:n.2846G>A
ENST00000639676.1:n.1678G>A
ENST00000640403.1:c.1371G>A ENSP00000492531.1:p.Trp457Ter
XM_011543675.1:c.4080G>A XP_011541977.1:p.Trp1360Ter
XM_011543676.1:c.4080G>A XP_011541978.1:p.Trp1360Ter
XM_011543677.1:c.1383G>A XP_011541979.1:p.Trp461Ter
XM_011543678.1:c.4080G>A XP_011541980.1:p.Trp1360Ter
XM_011543679.1:c.4080G>A XP_011541981.1:p.Trp1360Ter
XM_017009963.2:c.4080G>A XP_016865452.1:p.Trp1360Ter
XM_017009964.2:c.4080G>A XP_016865453.1:p.Trp1360Ter
XM_017009965.1:c.4077G>A XP_016865454.1:p.Trp1359Ter
XM_017009966.2:c.4080G>A XP_016865455.1:p.Trp1360Ter
XM_017009967.1:c.3984G>A XP_016865456.1:p.Trp1328Ter
XM_017009968.2:c.4080G>A XP_016865457.1:p.Trp1360Ter
XM_017009969.2:c.4080G>A XP_016865458.1:p.Trp1360Ter
XM_017009970.2:c.4080G>A XP_016865459.1:p.Trp1360Ter
XM_017009971.2:c.4080G>A XP_016865460.1:p.Trp1360Ter
XM_017009974.2:c.4080G>A XP_016865463.1:p.Trp1360Ter