Canonical Allele Identifier: CA360396199

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008143A>G (hg19) ; chr5:g.90712326A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712326A>G , CM000667.2:g.90712326A>G	GRCh38
NC_000005.9:g.90008143A>G , CM000667.1:g.90008143A>G	GRCh37
NC_000005.8:g.90043899A>G	NCBI36
NG_007083.1:g.158527A>G
NG_007083.2:g.187983A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9082A>G MANE Select	ENSP00000384582.2:p.Asn3028Asp
ENST00000639431.1:c.265+36117A>G	ENSP00000491057.1:n.265+36117A>G
ENST00000639473.1:n.4541A>G
ENST00000640012.1:c.2889A>G
ENST00000640374.1:n.2226A>G
ENST00000640779.1:c.3811A>G
ENST00000405460.6:c.9082A>G	ENSP00000384582.2:p.Asn3028Asp
ENST00000509621.1:c.1779A>G
NM_032119.3:c.9082A>G	NP_115495.3:p.Asn3028Asp
NR_003149.1:n.9095A>G
XM_011543675.1:c.9079A>G	XP_011541977.1:p.Asn3027Asp
XM_011543676.1:c.9001A>G	XP_011541978.1:p.Asn3001Asp
XM_011543677.1:c.6385A>G	XP_011541979.1:p.Asn2129Asp
XM_011543678.1:c.9082A>G	XP_011541980.1:p.Asn3028Asp
XM_011543679.1:c.9082A>G	XP_011541981.1:p.Asn3028Asp
NM_032119.4:c.9082A>G MANE Select	NP_115495.3:p.Asn3028Asp
XM_017009963.2:c.9103A>G	XP_016865452.1:p.Asn3035Asp
XM_017009964.2:c.9100A>G	XP_016865453.1:p.Asn3034Asp
XM_017009965.1:c.9100A>G	XP_016865454.1:p.Asn3034Asp
XM_017009966.2:c.9022A>G	XP_016865455.1:p.Asn3008Asp
XM_017009967.1:c.9007A>G	XP_016865456.1:p.Asn3003Asp
XM_017009968.2:c.9103A>G	XP_016865457.1:p.Asn3035Asp
XM_017009969.2:c.9103A>G	XP_016865458.1:p.Asn3035Asp
XM_017009970.2:c.9103A>G	XP_016865459.1:p.Asn3035Asp
XM_017009971.2:c.9103A>G	XP_016865460.1:p.Asn3035Asp
XM_017009972.1:c.2221A>G	XP_016865461.1:p.Asn741Asp
XM_017009973.1:c.2200A>G	XP_016865462.1:p.Asn734Asp
XM_017009974.2:c.9103A>G	XP_016865463.1:p.Asn3035Asp
NR_003149.2:n.9098A>G