Canonical Allele Identifier: CA138112

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90652488A>G , CM000667.2:g.90652488A>G	GRCh38
NC_000005.9:g.89948305A>G , CM000667.1:g.89948305A>G	GRCh37
NC_000005.8:g.89984061A>G	NCBI36
NG_007083.1:g.98689A>G
NG_007083.2:g.128145A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.3559A>G MANE Select	ENSP00000384582.2:p.Ile1187Val
ENST00000504142.2:n.2325A>G
ENST00000639676.1:n.1157A>G
ENST00000640403.1:c.862A>G	ENSP00000492531.1:p.Ile288Val
ENST00000405460.6:c.3559A>G	ENSP00000384582.2:p.Ile1187Val
ENST00000504142.1:c.2324A>G
NM_032119.3:c.3559A>G	NP_115495.3:p.Ile1187Val
NR_003149.1:n.3655A>G
XM_011543675.1:c.3559A>G	XP_011541977.1:p.Ile1187Val
XM_011543676.1:c.3559A>G	XP_011541978.1:p.Ile1187Val
XM_011543677.1:c.862A>G	XP_011541979.1:p.Ile288Val
XM_011543678.1:c.3559A>G	XP_011541980.1:p.Ile1187Val
XM_011543679.1:c.3559A>G	XP_011541981.1:p.Ile1187Val
NM_032119.4:c.3559A>G MANE Select	NP_115495.3:p.Ile1187Val
XM_017009963.2:c.3559A>G	XP_016865452.1:p.Ile1187Val
XM_017009964.2:c.3559A>G	XP_016865453.1:p.Ile1187Val
XM_017009965.1:c.3556A>G	XP_016865454.1:p.Ile1186Val
XM_017009966.2:c.3559A>G	XP_016865455.1:p.Ile1187Val
XM_017009967.1:c.3463A>G	XP_016865456.1:p.Ile1155Val
XM_017009968.2:c.3559A>G	XP_016865457.1:p.Ile1187Val
XM_017009969.2:c.3559A>G	XP_016865458.1:p.Ile1187Val
XM_017009970.2:c.3559A>G	XP_016865459.1:p.Ile1187Val
XM_017009971.2:c.3559A>G	XP_016865460.1:p.Ile1187Val
XM_017009974.2:c.3559A>G	XP_016865463.1:p.Ile1187Val
NR_003149.2:n.3658A>G