Canonical Allele Identifier: CA360401687
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90791204G>A , CM000667.2:g.90791204G>A GRCh38
NC_000005.9:g.90087021G>A , CM000667.1:g.90087021G>A GRCh37
NC_000005.8:g.90122777G>A NCBI36
NG_007083.1:g.237405G>A
NG_007083.2:g.266861G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.14375G>A MANE Select ENSP00000384582.2:p.Gly4792Glu
ENST00000425867.3:c.3329G>A ENSP00000392618.3:p.Gly1110Glu
ENST00000507314.2:c.50G>A ENSP00000491299.1:p.Gly17Glu
ENST00000638510.1:n.1642G>A
ENST00000638585.1:n.141G>A
ENST00000638975.1:c.1004G>A ENSP00000492630.1:p.Gly335Glu
ENST00000639431.1:c.265+114995G>A ENSP00000491057.1:n.265+114995G>A
ENST00000640407.1:c.785G>A ENSP00000491425.1:p.Gly262Glu
ENST00000405460.6:c.14375G>A ENSP00000384582.2:p.Gly4792Glu
ENST00000425867.2:c.1358G>A ENSP00000392618.2:p.Gly453Glu
ENST00000507314.1:n.50G>A
NM_032119.3:c.14375G>A NP_115495.3:p.Gly4792Glu
NR_003149.1:n.14388G>A
XM_011543675.1:c.14372G>A XP_011541977.1:p.Gly4791Glu
XM_011543676.1:c.14294G>A XP_011541978.1:p.Gly4765Glu
XM_011543677.1:c.11678G>A XP_011541979.1:p.Gly3893Glu
XM_011543678.1:c.14375G>A XP_011541980.1:p.Gly4792Glu
NM_032119.4:c.14375G>A MANE Select NP_115495.3:p.Gly4792Glu
XM_017009963.2:c.14396G>A XP_016865452.1:p.Gly4799Glu
XM_017009964.2:c.14393G>A XP_016865453.1:p.Gly4798Glu
XM_017009965.1:c.14393G>A XP_016865454.1:p.Gly4798Glu
XM_017009966.2:c.14315G>A XP_016865455.1:p.Gly4772Glu
XM_017009967.1:c.14300G>A XP_016865456.1:p.Gly4767Glu
XM_017009968.2:c.14396G>A XP_016865457.1:p.Gly4799Glu
XM_017009969.2:c.14396G>A XP_016865458.1:p.Gly4799Glu
XM_017009970.2:c.14396G>A XP_016865459.1:p.Gly4799Glu
XM_017009971.2:c.14396G>A XP_016865460.1:p.Gly4799Glu
XM_017009972.1:c.7514G>A XP_016865461.1:p.Gly2505Glu
XM_017009973.1:c.7493G>A XP_016865462.1:p.Gly2498Glu
NR_003149.2:n.14391G>A