Canonical Allele Identifier: CA360399405

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720075A>T , CM000667.2:g.90720075A>T	GRCh38
NC_000005.9:g.90015892A>T , CM000667.1:g.90015892A>T	GRCh37
NC_000005.8:g.90051648A>T	NCBI36
NG_007083.1:g.166276A>T
NG_007083.2:g.195732A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9475A>T MANE Select	NP_115495.3:p.Thr3159Ser
ENST00000405460.9:c.9475A>T MANE Select	ENSP00000384582.2:p.Thr3159Ser
NM_032119.3:c.9475A>T	NP_115495.3:p.Thr3159Ser
NR_003149.1:n.9488A>T
NR_003149.2:n.9491A>T
ENST00000405460.6:c.9475A>T	ENSP00000384582.2:p.Thr3159Ser
ENST00000509621.1:c.2172A>T
ENST00000639431.1:c.265+43866A>T	ENSP00000491057.1:n.265+43866A>T
ENST00000640374.1:n.2619A>T
ENST00000640779.1:c.4204A>T
XM_011543675.1:c.9472A>T	XP_011541977.1:p.Thr3158Ser
XM_011543676.1:c.9394A>T	XP_011541978.1:p.Thr3132Ser
XM_011543677.1:c.6778A>T	XP_011541979.1:p.Thr2260Ser
XM_011543678.1:c.9475A>T	XP_011541980.1:p.Thr3159Ser
XM_011543679.1:c.9475A>T	XP_011541981.1:p.Thr3159Ser
XM_017009963.2:c.9496A>T	XP_016865452.1:p.Thr3166Ser
XM_017009964.2:c.9493A>T	XP_016865453.1:p.Thr3165Ser
XM_017009965.1:c.9493A>T	XP_016865454.1:p.Thr3165Ser
XM_017009966.2:c.9415A>T	XP_016865455.1:p.Thr3139Ser
XM_017009967.1:c.9400A>T	XP_016865456.1:p.Thr3134Ser
XM_017009968.2:c.9496A>T	XP_016865457.1:p.Thr3166Ser
XM_017009969.2:c.9496A>T	XP_016865458.1:p.Thr3166Ser
XM_017009970.2:c.9496A>T	XP_016865459.1:p.Thr3166Ser
XM_017009971.2:c.9496A>T	XP_016865460.1:p.Thr3166Ser
XM_017009972.1:c.2614A>T	XP_016865461.1:p.Thr872Ser
XM_017009973.1:c.2593A>T	XP_016865462.1:p.Thr865Ser
XM_017009974.2:c.9496A>T	XP_016865463.1:p.Thr3166Ser
XR_001742802.1:n.2523-4266T>A
XR_948560.1:n.272-4266T>A