Canonical Allele Identifier: CA3339128

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90647697A>G , CM000667.2:g.90647697A>G	GRCh38
NC_000005.9:g.89943514A>G , CM000667.1:g.89943514A>G	GRCh37
NC_000005.8:g.89979270A>G	NCBI36
NG_007083.1:g.93898A>G
NG_007083.2:g.123354A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.3222A>G MANE Select	NP_115495.3:p.Ile1074Met
ENST00000405460.9:c.3222A>G MANE Select	ENSP00000384582.2:p.Ile1074Met
NM_032119.3:c.3222A>G	NP_115495.3:p.Ile1074Met
NR_003149.1:n.3318A>G
NR_003149.2:n.3321A>G
ENST00000405460.6:c.3222A>G	ENSP00000384582.2:p.Ile1074Met
ENST00000504142.1:c.1987A>G
ENST00000504142.2:n.1988A>G
ENST00000639676.1:n.820A>G
ENST00000640403.1:c.525A>G	ENSP00000492531.1:p.Ile175Met
XM_011543675.1:c.3222A>G	XP_011541977.1:p.Ile1074Met
XM_011543676.1:c.3222A>G	XP_011541978.1:p.Ile1074Met
XM_011543677.1:c.525A>G	XP_011541979.1:p.Ile175Met
XM_011543678.1:c.3222A>G	XP_011541980.1:p.Ile1074Met
XM_011543679.1:c.3222A>G	XP_011541981.1:p.Ile1074Met
XM_017009963.2:c.3222A>G	XP_016865452.1:p.Ile1074Met
XM_017009964.2:c.3222A>G	XP_016865453.1:p.Ile1074Met
XM_017009965.1:c.3219A>G	XP_016865454.1:p.Ile1073Met
XM_017009966.2:c.3222A>G	XP_016865455.1:p.Ile1074Met
XM_017009967.1:c.3126A>G	XP_016865456.1:p.Ile1042Met
XM_017009968.2:c.3222A>G	XP_016865457.1:p.Ile1074Met
XM_017009969.2:c.3222A>G	XP_016865458.1:p.Ile1074Met
XM_017009970.2:c.3222A>G	XP_016865459.1:p.Ile1074Met
XM_017009971.2:c.3222A>G	XP_016865460.1:p.Ile1074Met
XM_017009974.2:c.3222A>G	XP_016865463.1:p.Ile1074Met