Canonical Allele Identifier: CA3339761

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90685843A>G , CM000667.2:g.90685843A>G	GRCh38
NC_000005.9:g.89981660A>G , CM000667.1:g.89981660A>G	GRCh37
NC_000005.8:g.90017416A>G	NCBI36
NG_007083.1:g.132044A>G
NG_007083.2:g.161500A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.6338A>G MANE Select	NP_115495.3:p.Asn2113Ser
ENST00000405460.9:c.6338A>G MANE Select	ENSP00000384582.2:p.Asn2113Ser
NM_032119.3:c.6338A>G	NP_115495.3:p.Asn2113Ser
NR_003149.1:n.6434A>G
NR_003149.2:n.6437A>G
ENST00000405460.6:c.6338A>G	ENSP00000384582.2:p.Asn2113Ser
ENST00000639431.1:c.265+9634A>G	ENSP00000491057.1:n.265+9634A>G
ENST00000639473.1:n.1797A>G
ENST00000640012.1:c.228A>G
ENST00000640403.1:c.3629A>G	ENSP00000492531.1:p.Asn1210Ser
ENST00000640779.1:c.1150A>G
XM_011543675.1:c.6335A>G	XP_011541977.1:p.Asn2112Ser
XM_011543676.1:c.6257A>G	XP_011541978.1:p.Asn2086Ser
XM_011543677.1:c.3641A>G	XP_011541979.1:p.Asn1214Ser
XM_011543678.1:c.6338A>G	XP_011541980.1:p.Asn2113Ser
XM_011543679.1:c.6338A>G	XP_011541981.1:p.Asn2113Ser
XM_017009963.2:c.6338A>G	XP_016865452.1:p.Asn2113Ser
XM_017009964.2:c.6335A>G	XP_016865453.1:p.Asn2112Ser
XM_017009965.1:c.6335A>G	XP_016865454.1:p.Asn2112Ser
XM_017009966.2:c.6257A>G	XP_016865455.1:p.Asn2086Ser
XM_017009967.1:c.6242A>G	XP_016865456.1:p.Asn2081Ser
XM_017009968.2:c.6338A>G	XP_016865457.1:p.Asn2113Ser
XM_017009969.2:c.6338A>G	XP_016865458.1:p.Asn2113Ser
XM_017009970.2:c.6338A>G	XP_016865459.1:p.Asn2113Ser
XM_017009971.2:c.6338A>G	XP_016865460.1:p.Asn2113Ser
XM_017009973.1:c.-462A>G	XP_016865462.1:n.-462A>G
XM_017009974.2:c.6338A>G	XP_016865463.1:p.Asn2113Ser