Canonical Allele Identifier: CA3341859
Community Standard Title: NM_032119.4(ADGRV1):c.15009C>T (p.Gly5003=)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90810269C>T , CM000667.2:g.90810269C>T GRCh38
NC_000005.9:g.90106086C>T , CM000667.1:g.90106086C>T GRCh37
NC_000005.8:g.90141842C>T NCBI36
NG_007083.1:g.256470C>T
NG_007083.2:g.285926C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.15009C>T MANE Select NP_115495.3:p.Gly5003=
ENST00000405460.9:c.15009C>T MANE Select ENSP00000384582.2:p.Gly5003=
NM_032119.3:c.15009C>T NP_115495.3:p.Gly5003=
NR_003149.1:n.15022C>T
NR_003149.2:n.15025C>T
ENST00000405460.6:c.15009C>T ENSP00000384582.2:p.Gly5003=
ENST00000425867.2:c.1992C>T ENSP00000392618.2:p.Gly664=
ENST00000425867.3:c.3963C>T ENSP00000392618.3:p.Gly1321=
ENST00000638510.1:n.2276C>T
ENST00000638585.1:n.464C>T
ENST00000639431.1:c.265+134060C>T ENSP00000491057.1:n.265+134060C>T
ENST00000640407.1:c.1419C>T ENSP00000491425.1:p.Gly473=
XM_011543675.1:c.15006C>T XP_011541977.1:p.Gly5002=
XM_011543676.1:c.14928C>T XP_011541978.1:p.Gly4976=
XM_011543677.1:c.12312C>T XP_011541979.1:p.Gly4104=
XM_011543678.1:c.*16C>T XP_011541980.1:n.*16C>T
XM_017009963.2:c.15030C>T XP_016865452.1:p.Gly5010=
XM_017009964.2:c.15027C>T XP_016865453.1:p.Gly5009=
XM_017009965.1:c.15027C>T XP_016865454.1:p.Gly5009=
XM_017009966.2:c.14949C>T XP_016865455.1:p.Gly4983=
XM_017009967.1:c.14934C>T XP_016865456.1:p.Gly4978=
XM_017009968.2:c.14850C>T XP_016865457.1:p.Gly4950=
XM_017009969.2:c.15030C>T XP_016865458.1:p.Gly5010=
XM_017009970.2:c.*16C>T XP_016865459.1:n.*16C>T
XM_017009971.2:c.14855C>T XP_016865460.1:p.Ala4952Val
XM_017009972.1:c.8148C>T XP_016865461.1:p.Gly2716=
XM_017009973.1:c.8127C>T XP_016865462.1:p.Gly2709=