Canonical Allele Identifier: CA445409786

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90708890T>G , CM000667.2:g.90708890T>G	GRCh38
NC_000005.9:g.90004707T>G , CM000667.1:g.90004707T>G	GRCh37
NC_000005.8:g.90040463T>G	NCBI36
NG_007083.1:g.155091T>G
NG_007083.2:g.184547T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.8805T>G MANE Select	ENSP00000384582.2:p.Thr2935=
ENST00000639431.1:c.265+32681T>G	ENSP00000491057.1:n.265+32681T>G
ENST00000639473.1:n.4264T>G
ENST00000640012.1:c.2612T>G
ENST00000640374.1:n.1949T>G
ENST00000640403.1:c.6096T>G	ENSP00000492531.1:p.Thr2032=
ENST00000640779.1:c.3534T>G
ENST00000405460.6:c.8805T>G	ENSP00000384582.2:p.Thr2935=
ENST00000509621.1:c.1502T>G
NM_032119.3:c.8805T>G	NP_115495.3:p.Thr2935=
NR_003149.1:n.8818T>G
XM_011543675.1:c.8802T>G	XP_011541977.1:p.Thr2934=
XM_011543676.1:c.8724T>G	XP_011541978.1:p.Thr2908=
XM_011543677.1:c.6108T>G	XP_011541979.1:p.Thr2036=
XM_011543678.1:c.8805T>G	XP_011541980.1:p.Thr2935=
XM_011543679.1:c.8805T>G	XP_011541981.1:p.Thr2935=
NM_032119.4:c.8805T>G MANE Select	NP_115495.3:p.Thr2935=
XM_017009963.2:c.8826T>G	XP_016865452.1:p.Thr2942=
XM_017009964.2:c.8823T>G	XP_016865453.1:p.Thr2941=
XM_017009965.1:c.8823T>G	XP_016865454.1:p.Thr2941=
XM_017009966.2:c.8745T>G	XP_016865455.1:p.Thr2915=
XM_017009967.1:c.8730T>G	XP_016865456.1:p.Thr2910=
XM_017009968.2:c.8826T>G	XP_016865457.1:p.Thr2942=
XM_017009969.2:c.8826T>G	XP_016865458.1:p.Thr2942=
XM_017009970.2:c.8826T>G	XP_016865459.1:p.Thr2942=
XM_017009971.2:c.8826T>G	XP_016865460.1:p.Thr2942=
XM_017009972.1:c.1944T>G	XP_016865461.1:p.Thr648=
XM_017009973.1:c.1923T>G	XP_016865462.1:p.Thr641=
XM_017009974.2:c.8826T>G	XP_016865463.1:p.Thr2942=
NR_003149.2:n.8821T>G