Canonical Allele Identifier: CA360399402

Gene: ADGRV1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9475A>C MANE Select	NP_115495.3:p.Thr3159Pro
ENST00000405460.9:c.9475A>C MANE Select	ENSP00000384582.2:p.Thr3159Pro
NM_032119.3:c.9475A>C	NP_115495.3:p.Thr3159Pro
NR_003149.1:n.9488A>C
NR_003149.2:n.9491A>C
ENST00000405460.6:c.9475A>C	ENSP00000384582.2:p.Thr3159Pro
ENST00000509621.1:c.2172A>C
ENST00000639431.1:c.265+43866A>C	ENSP00000491057.1:n.265+43866A>C
ENST00000640374.1:n.2619A>C
ENST00000640779.1:c.4204A>C
XM_011543675.1:c.9472A>C	XP_011541977.1:p.Thr3158Pro
XM_011543676.1:c.9394A>C	XP_011541978.1:p.Thr3132Pro
XM_011543677.1:c.6778A>C	XP_011541979.1:p.Thr2260Pro
XM_011543678.1:c.9475A>C	XP_011541980.1:p.Thr3159Pro
XM_011543679.1:c.9475A>C	XP_011541981.1:p.Thr3159Pro
XM_017009963.2:c.9496A>C	XP_016865452.1:p.Thr3166Pro
XM_017009964.2:c.9493A>C	XP_016865453.1:p.Thr3165Pro
XM_017009965.1:c.9493A>C	XP_016865454.1:p.Thr3165Pro
XM_017009966.2:c.9415A>C	XP_016865455.1:p.Thr3139Pro
XM_017009967.1:c.9400A>C	XP_016865456.1:p.Thr3134Pro
XM_017009968.2:c.9496A>C	XP_016865457.1:p.Thr3166Pro
XM_017009969.2:c.9496A>C	XP_016865458.1:p.Thr3166Pro
XM_017009970.2:c.9496A>C	XP_016865459.1:p.Thr3166Pro
XM_017009971.2:c.9496A>C	XP_016865460.1:p.Thr3166Pro
XM_017009972.1:c.2614A>C	XP_016865461.1:p.Thr872Pro
XM_017009973.1:c.2593A>C	XP_016865462.1:p.Thr865Pro
XM_017009974.2:c.9496A>C	XP_016865463.1:p.Thr3166Pro
XR_001742802.1:n.2523-4266T>G
XR_948560.1:n.272-4266T>G