Canonical Allele Identifier: CA2709652128
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs2149721679

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90712181G>A , CM000667.2:g.90712181G>A GRCh38
NC_000005.9:g.90007998G>A , CM000667.1:g.90007998G>A GRCh37
NC_000005.8:g.90043754G>A NCBI36
NG_007083.1:g.158382G>A
NG_007083.2:g.187838G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.9043-106G>A MANE Select ENSP00000384582.2:n.9043-106G>A
ENST00000639431.1:c.265+35972G>A ENSP00000491057.1:n.265+35972G>A
ENST00000639473.1:n.4502-106G>A
ENST00000640012.1:c.2850-106G>A
ENST00000640374.1:n.2187-106G>A
ENST00000640779.1:c.3772-106G>A
ENST00000405460.6:c.9043-106G>A ENSP00000384582.2:n.9043-106G>A
ENST00000509621.1:c.1740-106G>A
NM_032119.3:c.9043-106G>A NP_115495.3:n.9043-106G>A
NR_003149.1:n.9056-106G>A
XM_011543675.1:c.9040-106G>A XP_011541977.1:n.9040-106G>A
XM_011543676.1:c.8962-106G>A XP_011541978.1:n.8962-106G>A
XM_011543677.1:c.6346-106G>A XP_011541979.1:n.6346-106G>A
XM_011543678.1:c.9043-106G>A XP_011541980.1:n.9043-106G>A
XM_011543679.1:c.9043-106G>A XP_011541981.1:n.9043-106G>A
NM_032119.4:c.9043-106G>A MANE Select NP_115495.3:n.9043-106G>A
XM_017009963.2:c.9064-106G>A XP_016865452.1:n.9064-106G>A
XM_017009964.2:c.9061-106G>A XP_016865453.1:n.9061-106G>A
XM_017009965.1:c.9061-106G>A XP_016865454.1:n.9061-106G>A
XM_017009966.2:c.8983-106G>A XP_016865455.1:n.8983-106G>A
XM_017009967.1:c.8968-106G>A XP_016865456.1:n.8968-106G>A
XM_017009968.2:c.9064-106G>A XP_016865457.1:n.9064-106G>A
XM_017009969.2:c.9064-106G>A XP_016865458.1:n.9064-106G>A
XM_017009970.2:c.9064-106G>A XP_016865459.1:n.9064-106G>A
XM_017009971.2:c.9064-106G>A XP_016865460.1:n.9064-106G>A
XM_017009972.1:c.2182-106G>A XP_016865461.1:n.2182-106G>A
XM_017009973.1:c.2161-106G>A XP_016865462.1:n.2161-106G>A
XM_017009974.2:c.9064-106G>A XP_016865463.1:n.9064-106G>A
NR_003149.2:n.9059-106G>A