Canonical Allele Identifier: CA1562829236
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627111C= , CM000667.2:g.90627111C= GRCh38
NC_000005.9:g.89922928C= , CM000667.1:g.89922928C= GRCh37
NC_000005.8:g.89958684C= NCBI36
NG_007083.1:g.73312C=
NG_007083.2:g.102768C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.673-100C= MANE Select ENSP00000384582.2:n.673-100C=
ENST00000640083.1:n.378-100C=
ENST00000640109.1:n.769-100C=
ENST00000640281.1:n.732-100C=
ENST00000405460.6:c.673-100C= ENSP00000384582.2:n.673-100C=
NM_032119.3:c.673-100C= NP_115495.3:n.673-100C=
NR_003149.1:n.769-100C=
XM_011543675.1:c.673-100C= XP_011541977.1:n.673-100C=
XM_011543676.1:c.673-100C= XP_011541978.1:n.673-100C=
XM_011543678.1:c.673-100C= XP_011541980.1:n.673-100C=
XM_011543679.1:c.673-100C= XP_011541981.1:n.673-100C=
NM_032119.4:c.673-100C= MANE Select NP_115495.3:n.673-100C=
XM_017009963.2:c.673-100C= XP_016865452.1:n.673-100C=
XM_017009964.2:c.673-100C= XP_016865453.1:n.673-100C=
XM_017009965.1:c.670-100C= XP_016865454.1:n.670-100C=
XM_017009966.2:c.673-100C= XP_016865455.1:n.673-100C=
XM_017009967.1:c.577-100C= XP_016865456.1:n.577-100C=
XM_017009968.2:c.673-100C= XP_016865457.1:n.673-100C=
XM_017009969.2:c.673-100C= XP_016865458.1:n.673-100C=
XM_017009970.2:c.673-100C= XP_016865459.1:n.673-100C=
XM_017009971.2:c.673-100C= XP_016865460.1:n.673-100C=
XM_017009974.2:c.673-100C= XP_016865463.1:n.673-100C=
NR_003149.2:n.772-100C=