Canonical Allele Identifier: CA123051477

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91153306C>T , CM000667.2:g.91153306C>T	GRCh38
NC_000005.9:g.90449123C>T , CM000667.1:g.90449123C>T	GRCh37
NC_000005.8:g.90484879C>T	NCBI36
NG_007083.1:g.599507C>T
NG_007083.2:g.628963C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18710C>T MANE Select	NP_115495.3:p.Thr6237Met
ENST00000405460.9:c.18710C>T MANE Select	ENSP00000384582.2:p.Thr6237Met
NM_032119.3:c.18710C>T	NP_115495.3:p.Thr6237Met
NR_003149.1:n.18723C>T
NR_003149.2:n.18726C>T
ENST00000405460.6:c.18710C>T	ENSP00000384582.2:p.Thr6237Met
ENST00000425867.2:c.5693C>T	ENSP00000392618.2:p.Thr1898Met
ENST00000425867.3:c.7664C>T	ENSP00000392618.3:p.Thr2555Met
ENST00000638510.1:n.5977C>T
ENST00000638990.1:c.1922C>T
ENST00000639212.1:n.630C>T
ENST00000639530.1:n.578C>T
ENST00000639821.1:c.517-10476C>T	ENSP00000492216.1:n.517-10476C>T
ENST00000640256.1:n.386C>T
ENST00000640407.1:c.5159C>T	ENSP00000491425.1:n.5159C>T
ENST00000640815.1:c.794C>T	ENSP00000491767.1:p.Thr265Met
XM_011543675.1:c.18707C>T	XP_011541977.1:p.Thr6236Met
XM_011543676.1:c.18629C>T	XP_011541978.1:p.Thr6210Met
XM_011543677.1:c.16013C>T	XP_011541979.1:p.Thr5338Met
XM_017009963.2:c.18731C>T	XP_016865452.1:p.Thr6244Met
XM_017009964.2:c.18728C>T	XP_016865453.1:p.Thr6243Met
XM_017009965.1:c.18728C>T	XP_016865454.1:p.Thr6243Met
XM_017009966.2:c.18650C>T	XP_016865455.1:p.Thr6217Met
XM_017009967.1:c.18635C>T	XP_016865456.1:p.Thr6212Met
XM_017009968.2:c.18551C>T	XP_016865457.1:p.Thr6184Met
XM_017009969.2:c.18454-10476C>T	XP_016865458.1:n.18454-10476C>T
XM_017009972.1:c.11849C>T	XP_016865461.1:p.Thr3950Met
XM_017009973.1:c.11828C>T	XP_016865462.1:p.Thr3943Met
XR_001742795.1:n.225-1118G>A
XR_001742796.1:n.225-17312G>A