Canonical Allele Identifier: CA3339531
Community Standard Title: NM_032119.4(ADGRV1):c.5311C>T (p.Gln1771Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90675443C>T , CM000667.2:g.90675443C>T GRCh38
NC_000005.9:g.89971260C>T , CM000667.1:g.89971260C>T GRCh37
NC_000005.8:g.90007016C>T NCBI36
NG_007083.1:g.121644C>T
NG_007083.2:g.151100C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.5311C>T MANE Select NP_115495.3:p.Gln1771Ter
ENST00000405460.9:c.5311C>T MANE Select ENSP00000384582.2:p.Gln1771Ter
NM_032119.3:c.5311C>T NP_115495.3:p.Gln1771Ter
NR_003149.1:n.5407C>T
NR_003149.2:n.5410C>T
ENST00000405460.6:c.5311C>T ENSP00000384582.2:p.Gln1771Ter
ENST00000450321.2:n.646C>T
ENST00000639431.1:c.133C>T ENSP00000491057.1:p.Gln45Ter
ENST00000639473.1:n.770C>T
ENST00000640403.1:c.2602C>T ENSP00000492531.1:p.Gln868Ter
ENST00000640779.1:c.126C>T
XM_011543675.1:c.5311C>T XP_011541977.1:p.Gln1771Ter
XM_011543676.1:c.5311C>T XP_011541978.1:p.Gln1771Ter
XM_011543677.1:c.2614C>T XP_011541979.1:p.Gln872Ter
XM_011543678.1:c.5311C>T XP_011541980.1:p.Gln1771Ter
XM_011543679.1:c.5311C>T XP_011541981.1:p.Gln1771Ter
XM_017009963.2:c.5311C>T XP_016865452.1:p.Gln1771Ter
XM_017009964.2:c.5311C>T XP_016865453.1:p.Gln1771Ter
XM_017009965.1:c.5308C>T XP_016865454.1:p.Gln1770Ter
XM_017009966.2:c.5311C>T XP_016865455.1:p.Gln1771Ter
XM_017009967.1:c.5215C>T XP_016865456.1:p.Gln1739Ter
XM_017009968.2:c.5311C>T XP_016865457.1:p.Gln1771Ter
XM_017009969.2:c.5311C>T XP_016865458.1:p.Gln1771Ter
XM_017009970.2:c.5311C>T XP_016865459.1:p.Gln1771Ter
XM_017009971.2:c.5311C>T XP_016865460.1:p.Gln1771Ter
XM_017009973.1:c.-1486C>T XP_016865462.1:n.-1486C>T
XM_017009974.2:c.5311C>T XP_016865463.1:p.Gln1771Ter