Canonical Allele Identifier: CA360397832
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90716728A>T , CM000667.2:g.90716728A>T GRCh38
NC_000005.9:g.90012545A>T , CM000667.1:g.90012545A>T GRCh37
NC_000005.8:g.90048301A>T NCBI36
NG_007083.1:g.162929A>T
NG_007083.2:g.192385A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.9446A>T MANE Select ENSP00000384582.2:p.Lys3149Met
ENST00000639431.1:c.265+40519A>T ENSP00000491057.1:n.265+40519A>T
ENST00000639473.1:n.4905A>T
ENST00000640374.1:n.2590A>T
ENST00000640779.1:c.4175A>T
ENST00000405460.6:c.9446A>T ENSP00000384582.2:p.Lys3149Met
ENST00000509621.1:c.2143A>T
NM_032119.3:c.9446A>T NP_115495.3:p.Lys3149Met
NR_003149.1:n.9459A>T
XM_011543675.1:c.9443A>T XP_011541977.1:p.Lys3148Met
XM_011543676.1:c.9365A>T XP_011541978.1:p.Lys3122Met
XM_011543677.1:c.6749A>T XP_011541979.1:p.Lys2250Met
XM_011543678.1:c.9446A>T XP_011541980.1:p.Lys3149Met
XM_011543679.1:c.9446A>T XP_011541981.1:p.Lys3149Met
XR_948560.1:n.272-919T>A
NM_032119.4:c.9446A>T MANE Select NP_115495.3:p.Lys3149Met
XM_017009963.2:c.9467A>T XP_016865452.1:p.Lys3156Met
XM_017009964.2:c.9464A>T XP_016865453.1:p.Lys3155Met
XM_017009965.1:c.9464A>T XP_016865454.1:p.Lys3155Met
XM_017009966.2:c.9386A>T XP_016865455.1:p.Lys3129Met
XM_017009967.1:c.9371A>T XP_016865456.1:p.Lys3124Met
XM_017009968.2:c.9467A>T XP_016865457.1:p.Lys3156Met
XM_017009969.2:c.9467A>T XP_016865458.1:p.Lys3156Met
XM_017009970.2:c.9467A>T XP_016865459.1:p.Lys3156Met
XM_017009971.2:c.9467A>T XP_016865460.1:p.Lys3156Met
XM_017009972.1:c.2585A>T XP_016865461.1:p.Lys862Met
XM_017009973.1:c.2564A>T XP_016865462.1:p.Lys855Met
XM_017009974.2:c.9467A>T XP_016865463.1:p.Lys3156Met
XR_001742802.1:n.2523-919T>A
NR_003149.2:n.9462A>T