Canonical Allele Identifier: CA122797200
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs575383036

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692888dup , CM000667.2:g.90692888dup GRCh38
NC_000005.9:g.89988705dup , CM000667.1:g.89988705dup GRCh37
NC_000005.8:g.90024461dup NCBI36
NG_007083.1:g.139089dup
NG_007083.2:g.168545dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.7133+102dup MANE Select ENSP00000384582.2:n.7133+102dup
ENST00000639431.1:c.265+16679dup ENSP00000491057.1:n.265+16679dup
ENST00000639473.1:n.2592+102dup
ENST00000640012.1:c.940+102dup
ENST00000640374.1:n.277+102dup
ENST00000640403.1:c.4424+102dup ENSP00000492531.1:n.4424+102dup
ENST00000640779.1:c.1862+102dup
ENST00000405460.6:c.7133+102dup ENSP00000384582.2:n.7133+102dup
NM_032119.3:c.7133+102dup NP_115495.3:n.7133+102dup
NR_003149.1:n.7146+102dup
XM_011543675.1:c.7130+102dup XP_011541977.1:n.7130+102dup
XM_011543676.1:c.7052+102dup XP_011541978.1:n.7052+102dup
XM_011543677.1:c.4436+102dup XP_011541979.1:n.4436+102dup
XM_011543678.1:c.7133+102dup XP_011541980.1:n.7133+102dup
XM_011543679.1:c.7133+102dup XP_011541981.1:n.7133+102dup
NM_032119.4:c.7133+102dup MANE Select NP_115495.3:n.7133+102dup
XM_017009963.2:c.7133+102dup XP_016865452.1:n.7133+102dup
XM_017009964.2:c.7130+102dup XP_016865453.1:n.7130+102dup
XM_017009965.1:c.7130+102dup XP_016865454.1:n.7130+102dup
XM_017009966.2:c.7052+102dup XP_016865455.1:n.7052+102dup
XM_017009967.1:c.7037+102dup XP_016865456.1:n.7037+102dup
XM_017009968.2:c.7133+102dup XP_016865457.1:n.7133+102dup
XM_017009969.2:c.7133+102dup XP_016865458.1:n.7133+102dup
XM_017009970.2:c.7133+102dup XP_016865459.1:n.7133+102dup
XM_017009971.2:c.7133+102dup XP_016865460.1:n.7133+102dup
XM_017009972.1:c.251+102dup XP_016865461.1:n.251+102dup
XM_017009973.1:c.251+102dup XP_016865462.1:n.251+102dup
XM_017009974.2:c.7133+102dup XP_016865463.1:n.7133+102dup
NR_003149.2:n.7149+102dup