Canonical Allele Identifier: CA3340532

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720157C>A , CM000667.2:g.90720157C>A	GRCh38
NC_000005.9:g.90015974C>A , CM000667.1:g.90015974C>A	GRCh37
NC_000005.8:g.90051730C>A	NCBI36
NG_007083.1:g.166358C>A
NG_007083.2:g.195814C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9557C>A MANE Select	NP_115495.3:p.Thr3186Asn
ENST00000405460.9:c.9557C>A MANE Select	ENSP00000384582.2:p.Thr3186Asn
NM_032119.3:c.9557C>A	NP_115495.3:p.Thr3186Asn
NR_003149.1:n.9570C>A
NR_003149.2:n.9573C>A
ENST00000405460.6:c.9557C>A	ENSP00000384582.2:p.Thr3186Asn
ENST00000509621.1:c.2254C>A
ENST00000639431.1:c.265+43948C>A	ENSP00000491057.1:n.265+43948C>A
ENST00000640374.1:n.2701C>A
ENST00000640779.1:c.4286C>A
XM_011543675.1:c.9554C>A	XP_011541977.1:p.Thr3185Asn
XM_011543676.1:c.9476C>A	XP_011541978.1:p.Thr3159Asn
XM_011543677.1:c.6860C>A	XP_011541979.1:p.Thr2287Asn
XM_011543678.1:c.9557C>A	XP_011541980.1:p.Thr3186Asn
XM_011543679.1:c.9557C>A	XP_011541981.1:p.Thr3186Asn
XM_017009963.2:c.9578C>A	XP_016865452.1:p.Thr3193Asn
XM_017009964.2:c.9575C>A	XP_016865453.1:p.Thr3192Asn
XM_017009965.1:c.9575C>A	XP_016865454.1:p.Thr3192Asn
XM_017009966.2:c.9497C>A	XP_016865455.1:p.Thr3166Asn
XM_017009967.1:c.9482C>A	XP_016865456.1:p.Thr3161Asn
XM_017009968.2:c.9578C>A	XP_016865457.1:p.Thr3193Asn
XM_017009969.2:c.9578C>A	XP_016865458.1:p.Thr3193Asn
XM_017009970.2:c.9578C>A	XP_016865459.1:p.Thr3193Asn
XM_017009971.2:c.9578C>A	XP_016865460.1:p.Thr3193Asn
XM_017009972.1:c.2696C>A	XP_016865461.1:p.Thr899Asn
XM_017009973.1:c.2675C>A	XP_016865462.1:p.Thr892Asn
XM_017009974.2:c.9578C>A	XP_016865463.1:p.Thr3193Asn
XR_001742802.1:n.2523-4348G>T
XR_948560.1:n.272-4348G>T