Canonical Allele Identifier: CA360401723
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90791213G>A , CM000667.2:g.90791213G>A GRCh38
NC_000005.9:g.90087030G>A , CM000667.1:g.90087030G>A GRCh37
NC_000005.8:g.90122786G>A NCBI36
NG_007083.1:g.237414G>A
NG_007083.2:g.266870G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.14384G>A MANE Select ENSP00000384582.2:p.Gly4795Glu
ENST00000425867.3:c.3338G>A ENSP00000392618.3:p.Gly1113Glu
ENST00000507314.2:c.59G>A ENSP00000491299.1:p.Gly20Glu
ENST00000638510.1:n.1651G>A
ENST00000638585.1:n.150G>A
ENST00000638975.1:c.1013G>A ENSP00000492630.1:p.Gly338Glu
ENST00000639431.1:c.265+115004G>A ENSP00000491057.1:n.265+115004G>A
ENST00000640407.1:c.794G>A ENSP00000491425.1:p.Gly265Glu
ENST00000405460.6:c.14384G>A ENSP00000384582.2:p.Gly4795Glu
ENST00000425867.2:c.1367G>A ENSP00000392618.2:p.Gly456Glu
ENST00000507314.1:n.59G>A
NM_032119.3:c.14384G>A NP_115495.3:p.Gly4795Glu
NR_003149.1:n.14397G>A
XM_011543675.1:c.14381G>A XP_011541977.1:p.Gly4794Glu
XM_011543676.1:c.14303G>A XP_011541978.1:p.Gly4768Glu
XM_011543677.1:c.11687G>A XP_011541979.1:p.Gly3896Glu
XM_011543678.1:c.14384G>A XP_011541980.1:p.Gly4795Glu
NM_032119.4:c.14384G>A MANE Select NP_115495.3:p.Gly4795Glu
XM_017009963.2:c.14405G>A XP_016865452.1:p.Gly4802Glu
XM_017009964.2:c.14402G>A XP_016865453.1:p.Gly4801Glu
XM_017009965.1:c.14402G>A XP_016865454.1:p.Gly4801Glu
XM_017009966.2:c.14324G>A XP_016865455.1:p.Gly4775Glu
XM_017009967.1:c.14309G>A XP_016865456.1:p.Gly4770Glu
XM_017009968.2:c.14405G>A XP_016865457.1:p.Gly4802Glu
XM_017009969.2:c.14405G>A XP_016865458.1:p.Gly4802Glu
XM_017009970.2:c.14405G>A XP_016865459.1:p.Gly4802Glu
XM_017009971.2:c.14405G>A XP_016865460.1:p.Gly4802Glu
XM_017009972.1:c.7523G>A XP_016865461.1:p.Gly2508Glu
XM_017009973.1:c.7502G>A XP_016865462.1:p.Gly2501Glu
NR_003149.2:n.14400G>A