Canonical Allele Identifier: CA360406003

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90729765G>A , CM000667.2:g.90729765G>A	GRCh38
NC_000005.9:g.90025582G>A , CM000667.1:g.90025582G>A	GRCh37
NC_000005.8:g.90061338G>A	NCBI36
NG_007083.1:g.175966G>A
NG_007083.2:g.205422G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10549+1G>A MANE Select	NP_115495.3:n.10549+1G>A
ENST00000405460.9:c.10549+1G>A MANE Select	ENSP00000384582.2:n.10549+1G>A
NM_032119.3:c.10549+1G>A	NP_115495.3:n.10549+1G>A
NR_003149.1:n.10562+1G>A
NR_003149.2:n.10565+1G>A
ENST00000405460.6:c.10549+1G>A	ENSP00000384582.2:n.10549+1G>A
ENST00000509621.1:c.3246+1G>A
ENST00000639431.1:c.265+53556G>A	ENSP00000491057.1:n.265+53556G>A
ENST00000640374.1:n.3693+1G>A
ENST00000640464.1:n.968+1G>A
XM_011543675.1:c.10546+1G>A	XP_011541977.1:n.10546+1G>A
XM_011543676.1:c.10468+1G>A	XP_011541978.1:n.10468+1G>A
XM_011543677.1:c.7852+1G>A	XP_011541979.1:n.7852+1G>A
XM_011543678.1:c.10549+1G>A	XP_011541980.1:n.10549+1G>A
XM_011543679.1:c.10549+1G>A	XP_011541981.1:n.10549+1G>A
XM_017009963.2:c.10570+1G>A	XP_016865452.1:n.10570+1G>A
XM_017009964.2:c.10567+1G>A	XP_016865453.1:n.10567+1G>A
XM_017009965.1:c.10567+1G>A	XP_016865454.1:n.10567+1G>A
XM_017009966.2:c.10489+1G>A	XP_016865455.1:n.10489+1G>A
XM_017009967.1:c.10474+1G>A	XP_016865456.1:n.10474+1G>A
XM_017009968.2:c.10570+1G>A	XP_016865457.1:n.10570+1G>A
XM_017009969.2:c.10570+1G>A	XP_016865458.1:n.10570+1G>A
XM_017009970.2:c.10570+1G>A	XP_016865459.1:n.10570+1G>A
XM_017009971.2:c.10570+1G>A	XP_016865460.1:n.10570+1G>A
XM_017009972.1:c.3688+1G>A	XP_016865461.1:n.3688+1G>A
XM_017009973.1:c.3667+1G>A	XP_016865462.1:n.3667+1G>A
XM_017009974.2:c.10570+1G>A	XP_016865463.1:n.10570+1G>A
XR_001742802.1:n.2522+11142C>T
XR_948560.1:n.271+11142C>T