Canonical Allele Identifier: CA360401718
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90791212G>A , CM000667.2:g.90791212G>A GRCh38
NC_000005.9:g.90087029G>A , CM000667.1:g.90087029G>A GRCh37
NC_000005.8:g.90122785G>A NCBI36
NG_007083.1:g.237413G>A
NG_007083.2:g.266869G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.14383G>A MANE Select ENSP00000384582.2:p.Gly4795Arg
ENST00000425867.3:c.3337G>A ENSP00000392618.3:p.Gly1113Arg
ENST00000507314.2:c.58G>A ENSP00000491299.1:p.Gly20Arg
ENST00000638510.1:n.1650G>A
ENST00000638585.1:n.149G>A
ENST00000638975.1:c.1012G>A ENSP00000492630.1:p.Gly338Arg
ENST00000639431.1:c.265+115003G>A ENSP00000491057.1:n.265+115003G>A
ENST00000640407.1:c.793G>A ENSP00000491425.1:p.Gly265Arg
ENST00000405460.6:c.14383G>A ENSP00000384582.2:p.Gly4795Arg
ENST00000425867.2:c.1366G>A ENSP00000392618.2:p.Gly456Arg
ENST00000507314.1:n.58G>A
NM_032119.3:c.14383G>A NP_115495.3:p.Gly4795Arg
NR_003149.1:n.14396G>A
XM_011543675.1:c.14380G>A XP_011541977.1:p.Gly4794Arg
XM_011543676.1:c.14302G>A XP_011541978.1:p.Gly4768Arg
XM_011543677.1:c.11686G>A XP_011541979.1:p.Gly3896Arg
XM_011543678.1:c.14383G>A XP_011541980.1:p.Gly4795Arg
NM_032119.4:c.14383G>A MANE Select NP_115495.3:p.Gly4795Arg
XM_017009963.2:c.14404G>A XP_016865452.1:p.Gly4802Arg
XM_017009964.2:c.14401G>A XP_016865453.1:p.Gly4801Arg
XM_017009965.1:c.14401G>A XP_016865454.1:p.Gly4801Arg
XM_017009966.2:c.14323G>A XP_016865455.1:p.Gly4775Arg
XM_017009967.1:c.14308G>A XP_016865456.1:p.Gly4770Arg
XM_017009968.2:c.14404G>A XP_016865457.1:p.Gly4802Arg
XM_017009969.2:c.14404G>A XP_016865458.1:p.Gly4802Arg
XM_017009970.2:c.14404G>A XP_016865459.1:p.Gly4802Arg
XM_017009971.2:c.14404G>A XP_016865460.1:p.Gly4802Arg
XM_017009972.1:c.7522G>A XP_016865461.1:p.Gly2508Arg
XM_017009973.1:c.7501G>A XP_016865462.1:p.Gly2501Arg
NR_003149.2:n.14399G>A