Canonical Allele Identifier: CA3340725

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90728815A>T , CM000667.2:g.90728815A>T	GRCh38
NC_000005.9:g.90024632A>T , CM000667.1:g.90024632A>T	GRCh37
NC_000005.8:g.90060388A>T	NCBI36
NG_007083.1:g.175016A>T
NG_007083.2:g.204472A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.10308A>T MANE Select	NP_115495.3:p.Arg3436Ser
ENST00000405460.9:c.10308A>T MANE Select	ENSP00000384582.2:p.Arg3436Ser
NM_032119.3:c.10308A>T	NP_115495.3:p.Arg3436Ser
NR_003149.1:n.10321A>T
NR_003149.2:n.10324A>T
ENST00000405460.6:c.10308A>T	ENSP00000384582.2:p.Arg3436Ser
ENST00000509621.1:c.3005A>T
ENST00000639431.1:c.265+52606A>T	ENSP00000491057.1:n.265+52606A>T
ENST00000640374.1:n.3452A>T
ENST00000640464.1:n.727A>T
XM_011543675.1:c.10305A>T	XP_011541977.1:p.Arg3435Ser
XM_011543676.1:c.10227A>T	XP_011541978.1:p.Arg3409Ser
XM_011543677.1:c.7611A>T	XP_011541979.1:p.Arg2537Ser
XM_011543678.1:c.10308A>T	XP_011541980.1:p.Arg3436Ser
XM_011543679.1:c.10308A>T	XP_011541981.1:p.Arg3436Ser
XM_017009963.2:c.10329A>T	XP_016865452.1:p.Arg3443Ser
XM_017009964.2:c.10326A>T	XP_016865453.1:p.Arg3442Ser
XM_017009965.1:c.10326A>T	XP_016865454.1:p.Arg3442Ser
XM_017009966.2:c.10248A>T	XP_016865455.1:p.Arg3416Ser
XM_017009967.1:c.10233A>T	XP_016865456.1:p.Arg3411Ser
XM_017009968.2:c.10329A>T	XP_016865457.1:p.Arg3443Ser
XM_017009969.2:c.10329A>T	XP_016865458.1:p.Arg3443Ser
XM_017009970.2:c.10329A>T	XP_016865459.1:p.Arg3443Ser
XM_017009971.2:c.10329A>T	XP_016865460.1:p.Arg3443Ser
XM_017009972.1:c.3447A>T	XP_016865461.1:p.Arg1149Ser
XM_017009973.1:c.3426A>T	XP_016865462.1:p.Arg1142Ser
XM_017009974.2:c.10329A>T	XP_016865463.1:p.Arg3443Ser
XR_001742802.1:n.2522+12092T>A
XR_948560.1:n.271+12092T>A