Canonical Allele Identifier: CA1562863825
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90703610A= , CM000667.2:g.90703610A= GRCh38
NC_000005.9:g.89999427A= , CM000667.1:g.89999427A= GRCh37
NC_000005.8:g.90035183A= NCBI36
NG_007083.1:g.149811A=
NG_007083.2:g.179267A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.8156-55A= MANE Select ENSP00000384582.2:n.8156-55A=
ENST00000639431.1:c.265+27401A= ENSP00000491057.1:n.265+27401A=
ENST00000639473.1:n.3615-55A=
ENST00000640012.1:c.1963-55A=
ENST00000640374.1:n.1300-55A=
ENST00000640403.1:c.5447-55A= ENSP00000492531.1:n.5447-55A=
ENST00000640779.1:c.2885-55A=
ENST00000405460.6:c.8156-55A= ENSP00000384582.2:n.8156-55A=
ENST00000509621.1:c.853-55A=
NM_032119.3:c.8156-55A= NP_115495.3:n.8156-55A=
NR_003149.1:n.8169-55A=
XM_011543675.1:c.8153-55A= XP_011541977.1:n.8153-55A=
XM_011543676.1:c.8075-55A= XP_011541978.1:n.8075-55A=
XM_011543677.1:c.5459-55A= XP_011541979.1:n.5459-55A=
XM_011543678.1:c.8156-55A= XP_011541980.1:n.8156-55A=
XM_011543679.1:c.8156-55A= XP_011541981.1:n.8156-55A=
NM_032119.4:c.8156-55A= MANE Select NP_115495.3:n.8156-55A=
XM_017009963.2:c.8156-55A= XP_016865452.1:n.8156-55A=
XM_017009964.2:c.8153-55A= XP_016865453.1:n.8153-55A=
XM_017009965.1:c.8153-55A= XP_016865454.1:n.8153-55A=
XM_017009966.2:c.8075-55A= XP_016865455.1:n.8075-55A=
XM_017009967.1:c.8060-55A= XP_016865456.1:n.8060-55A=
XM_017009968.2:c.8156-55A= XP_016865457.1:n.8156-55A=
XM_017009969.2:c.8156-55A= XP_016865458.1:n.8156-55A=
XM_017009970.2:c.8156-55A= XP_016865459.1:n.8156-55A=
XM_017009971.2:c.8156-55A= XP_016865460.1:n.8156-55A=
XM_017009972.1:c.1274-55A= XP_016865461.1:n.1274-55A=
XM_017009973.1:c.1274-55A= XP_016865462.1:n.1274-55A=
XM_017009974.2:c.8156-55A= XP_016865463.1:n.8156-55A=
NR_003149.2:n.8172-55A=