Canonical Allele Identifier: CA3340710

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728735G>A , CM000667.2:g.90728735G>A	GRCh38
NC_000005.9:g.90024552G>A , CM000667.1:g.90024552G>A	GRCh37
NC_000005.8:g.90060308G>A	NCBI36
NG_007083.1:g.174936G>A
NG_007083.2:g.204392G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10228G>A MANE Select	NP_115495.3:p.Val3410Met
ENST00000405460.9:c.10228G>A MANE Select	ENSP00000384582.2:p.Val3410Met
NM_032119.3:c.10228G>A	NP_115495.3:p.Val3410Met
NR_003149.1:n.10241G>A
NR_003149.2:n.10244G>A
ENST00000405460.6:c.10228G>A	ENSP00000384582.2:p.Val3410Met
ENST00000509621.1:c.2925G>A
ENST00000639431.1:c.265+52526G>A	ENSP00000491057.1:n.265+52526G>A
ENST00000640374.1:n.3372G>A
ENST00000640464.1:n.647G>A
XM_011543675.1:c.10225G>A	XP_011541977.1:p.Val3409Met
XM_011543676.1:c.10147G>A	XP_011541978.1:p.Val3383Met
XM_011543677.1:c.7531G>A	XP_011541979.1:p.Val2511Met
XM_011543678.1:c.10228G>A	XP_011541980.1:p.Val3410Met
XM_011543679.1:c.10228G>A	XP_011541981.1:p.Val3410Met
XM_017009963.2:c.10249G>A	XP_016865452.1:p.Val3417Met
XM_017009964.2:c.10246G>A	XP_016865453.1:p.Val3416Met
XM_017009965.1:c.10246G>A	XP_016865454.1:p.Val3416Met
XM_017009966.2:c.10168G>A	XP_016865455.1:p.Val3390Met
XM_017009967.1:c.10153G>A	XP_016865456.1:p.Val3385Met
XM_017009968.2:c.10249G>A	XP_016865457.1:p.Val3417Met
XM_017009969.2:c.10249G>A	XP_016865458.1:p.Val3417Met
XM_017009970.2:c.10249G>A	XP_016865459.1:p.Val3417Met
XM_017009971.2:c.10249G>A	XP_016865460.1:p.Val3417Met
XM_017009972.1:c.3367G>A	XP_016865461.1:p.Val1123Met
XM_017009973.1:c.3346G>A	XP_016865462.1:p.Val1116Met
XM_017009974.2:c.10249G>A	XP_016865463.1:p.Val3417Met
XR_001742802.1:n.2522+12172C>T
XR_948560.1:n.271+12172C>T