Canonical Allele Identifier: CA360407689

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745091G>A , CM000667.2:g.90745091G>A	GRCh38
NC_000005.9:g.90040908G>A , CM000667.1:g.90040908G>A	GRCh37
NC_000005.8:g.90076664G>A	NCBI36
NG_007083.1:g.191292G>A
NG_007083.2:g.220748G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10595G>A MANE Select	NP_115495.3:p.Trp3532Ter
ENST00000405460.9:c.10595G>A MANE Select	ENSP00000384582.2:p.Trp3532Ter
NM_032119.3:c.10595G>A	NP_115495.3:p.Trp3532Ter
NR_003149.1:n.10608G>A
NR_003149.2:n.10611G>A
ENST00000405460.6:c.10595G>A	ENSP00000384582.2:p.Trp3532Ter
ENST00000509621.1:c.3292G>A
ENST00000639431.1:c.265+68882G>A	ENSP00000491057.1:n.265+68882G>A
ENST00000640374.1:n.3739G>A
ENST00000640464.1:n.1014G>A
XM_011543675.1:c.10592G>A	XP_011541977.1:p.Trp3531Ter
XM_011543676.1:c.10514G>A	XP_011541978.1:p.Trp3505Ter
XM_011543677.1:c.7898G>A	XP_011541979.1:p.Trp2633Ter
XM_011543678.1:c.10595G>A	XP_011541980.1:p.Trp3532Ter
XM_011543679.1:c.10595G>A	XP_011541981.1:p.Trp3532Ter
XM_017009963.2:c.10616G>A	XP_016865452.1:p.Trp3539Ter
XM_017009964.2:c.10613G>A	XP_016865453.1:p.Trp3538Ter
XM_017009965.1:c.10613G>A	XP_016865454.1:p.Trp3538Ter
XM_017009966.2:c.10535G>A	XP_016865455.1:p.Trp3512Ter
XM_017009967.1:c.10520G>A	XP_016865456.1:p.Trp3507Ter
XM_017009968.2:c.10616G>A	XP_016865457.1:p.Trp3539Ter
XM_017009969.2:c.10616G>A	XP_016865458.1:p.Trp3539Ter
XM_017009970.2:c.10616G>A	XP_016865459.1:p.Trp3539Ter
XM_017009971.2:c.10616G>A	XP_016865460.1:p.Trp3539Ter
XM_017009972.1:c.3734G>A	XP_016865461.1:p.Trp1245Ter
XM_017009973.1:c.3713G>A	XP_016865462.1:p.Trp1238Ter
XM_017009974.2:c.10616G>A	XP_016865463.1:p.Trp3539Ter