Canonical Allele Identifier: CA1562863818
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90703576_90703580delinsTTGCA , CM000667.2:g.90703576_90703580delinsTTGCA GRCh38
NC_000005.9:g.89999393_89999397delinsTTGCA , CM000667.1:g.89999393_89999397delinsTTGCA GRCh37
NC_000005.8:g.90035149_90035153delinsTTGCA NCBI36
NG_007083.1:g.149777_149781delinsTTGCA
NG_007083.2:g.179233_179237delinsTTGCA

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.8156-89_8156-85delinsTTGCA MANE Select ENSP00000384582.2:n.8156-89_8156-85delinsTTGCA
ENST00000639431.1:c.265+27367_265+27371delinsTTGCA ENSP00000491057.1:n.265+27367_265+27371delinsTTGCA
ENST00000639473.1:n.3615-89_3615-85delinsTTGCA
ENST00000640012.1:c.1963-89_1963-85delinsTTGCA
ENST00000640374.1:n.1300-89_1300-85delinsTTGCA
ENST00000640403.1:c.5447-89_5447-85delinsTTGCA ENSP00000492531.1:n.5447-89_5447-85delinsTTGCA
ENST00000640779.1:c.2885-89_2885-85delinsTTGCA
ENST00000405460.6:c.8156-89_8156-85delinsTTGCA ENSP00000384582.2:n.8156-89_8156-85delinsTTGCA
ENST00000509621.1:c.853-89_853-85delinsTTGCA
NM_032119.3:c.8156-89_8156-85delinsTTGCA NP_115495.3:n.8156-89_8156-85delinsTTGCA
NR_003149.1:n.8169-89_8169-85delinsTTGCA
XM_011543675.1:c.8153-89_8153-85delinsTTGCA XP_011541977.1:n.8153-89_8153-85delinsTTGCA
XM_011543676.1:c.8075-89_8075-85delinsTTGCA XP_011541978.1:n.8075-89_8075-85delinsTTGCA
XM_011543677.1:c.5459-89_5459-85delinsTTGCA XP_011541979.1:n.5459-89_5459-85delinsTTGCA
XM_011543678.1:c.8156-89_8156-85delinsTTGCA XP_011541980.1:n.8156-89_8156-85delinsTTGCA
XM_011543679.1:c.8156-89_8156-85delinsTTGCA XP_011541981.1:n.8156-89_8156-85delinsTTGCA
NM_032119.4:c.8156-89_8156-85delinsTTGCA MANE Select NP_115495.3:n.8156-89_8156-85delinsTTGCA
XM_017009963.2:c.8156-89_8156-85delinsTTGCA XP_016865452.1:n.8156-89_8156-85delinsTTGCA
XM_017009964.2:c.8153-89_8153-85delinsTTGCA XP_016865453.1:n.8153-89_8153-85delinsTTGCA
XM_017009965.1:c.8153-89_8153-85delinsTTGCA XP_016865454.1:n.8153-89_8153-85delinsTTGCA
XM_017009966.2:c.8075-89_8075-85delinsTTGCA XP_016865455.1:n.8075-89_8075-85delinsTTGCA
XM_017009967.1:c.8060-89_8060-85delinsTTGCA XP_016865456.1:n.8060-89_8060-85delinsTTGCA
XM_017009968.2:c.8156-89_8156-85delinsTTGCA XP_016865457.1:n.8156-89_8156-85delinsTTGCA
XM_017009969.2:c.8156-89_8156-85delinsTTGCA XP_016865458.1:n.8156-89_8156-85delinsTTGCA
XM_017009970.2:c.8156-89_8156-85delinsTTGCA XP_016865459.1:n.8156-89_8156-85delinsTTGCA
XM_017009971.2:c.8156-89_8156-85delinsTTGCA XP_016865460.1:n.8156-89_8156-85delinsTTGCA
XM_017009972.1:c.1274-89_1274-85delinsTTGCA XP_016865461.1:n.1274-89_1274-85delinsTTGCA
XM_017009973.1:c.1274-89_1274-85delinsTTGCA XP_016865462.1:n.1274-89_1274-85delinsTTGCA
XM_017009974.2:c.8156-89_8156-85delinsTTGCA XP_016865463.1:n.8156-89_8156-85delinsTTGCA
NR_003149.2:n.8172-89_8172-85delinsTTGCA