Canonical Allele Identifier: CA360396216
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90712333T>A , CM000667.2:g.90712333T>A GRCh38
NC_000005.9:g.90008150T>A , CM000667.1:g.90008150T>A GRCh37
NC_000005.8:g.90043906T>A NCBI36
NG_007083.1:g.158534T>A
NG_007083.2:g.187990T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.9089T>A MANE Select ENSP00000384582.2:p.Met3030Lys
ENST00000639431.1:c.265+36124T>A ENSP00000491057.1:n.265+36124T>A
ENST00000639473.1:n.4548T>A
ENST00000640012.1:c.2896T>A
ENST00000640374.1:n.2233T>A
ENST00000640779.1:c.3818T>A
ENST00000405460.6:c.9089T>A ENSP00000384582.2:p.Met3030Lys
ENST00000509621.1:c.1786T>A
NM_032119.3:c.9089T>A NP_115495.3:p.Met3030Lys
NR_003149.1:n.9102T>A
XM_011543675.1:c.9086T>A XP_011541977.1:p.Met3029Lys
XM_011543676.1:c.9008T>A XP_011541978.1:p.Met3003Lys
XM_011543677.1:c.6392T>A XP_011541979.1:p.Met2131Lys
XM_011543678.1:c.9089T>A XP_011541980.1:p.Met3030Lys
XM_011543679.1:c.9089T>A XP_011541981.1:p.Met3030Lys
NM_032119.4:c.9089T>A MANE Select NP_115495.3:p.Met3030Lys
XM_017009963.2:c.9110T>A XP_016865452.1:p.Met3037Lys
XM_017009964.2:c.9107T>A XP_016865453.1:p.Met3036Lys
XM_017009965.1:c.9107T>A XP_016865454.1:p.Met3036Lys
XM_017009966.2:c.9029T>A XP_016865455.1:p.Met3010Lys
XM_017009967.1:c.9014T>A XP_016865456.1:p.Met3005Lys
XM_017009968.2:c.9110T>A XP_016865457.1:p.Met3037Lys
XM_017009969.2:c.9110T>A XP_016865458.1:p.Met3037Lys
XM_017009970.2:c.9110T>A XP_016865459.1:p.Met3037Lys
XM_017009971.2:c.9110T>A XP_016865460.1:p.Met3037Lys
XM_017009972.1:c.2228T>A XP_016865461.1:p.Met743Lys
XM_017009973.1:c.2207T>A XP_016865462.1:p.Met736Lys
XM_017009974.2:c.9110T>A XP_016865463.1:p.Met3037Lys
NR_003149.2:n.9105T>A