Canonical Allele Identifier: CA360402828

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725097A>G , CM000667.2:g.90725097A>G	GRCh38
NC_000005.9:g.90020914A>G , CM000667.1:g.90020914A>G	GRCh37
NC_000005.8:g.90056670A>G	NCBI36
NG_007083.1:g.171298A>G
NG_007083.2:g.200754A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9918A>G MANE Select	NP_115495.3:p.Ile3306Met
ENST00000405460.9:c.9918A>G MANE Select	ENSP00000384582.2:p.Ile3306Met
NM_032119.3:c.9918A>G	NP_115495.3:p.Ile3306Met
NR_003149.1:n.9931A>G
NR_003149.2:n.9934A>G
ENST00000405460.6:c.9918A>G	ENSP00000384582.2:p.Ile3306Met
ENST00000509621.1:c.2615A>G
ENST00000639431.1:c.265+48888A>G	ENSP00000491057.1:n.265+48888A>G
ENST00000640374.1:n.3062A>G
ENST00000640464.1:n.337A>G
ENST00000640779.1:c.4647A>G
XM_011543675.1:c.9915A>G	XP_011541977.1:p.Ile3305Met
XM_011543676.1:c.9837A>G	XP_011541978.1:p.Ile3279Met
XM_011543677.1:c.7221A>G	XP_011541979.1:p.Ile2407Met
XM_011543678.1:c.9918A>G	XP_011541980.1:p.Ile3306Met
XM_011543679.1:c.9918A>G	XP_011541981.1:p.Ile3306Met
XM_017009963.2:c.9939A>G	XP_016865452.1:p.Ile3313Met
XM_017009964.2:c.9936A>G	XP_016865453.1:p.Ile3312Met
XM_017009965.1:c.9936A>G	XP_016865454.1:p.Ile3312Met
XM_017009966.2:c.9858A>G	XP_016865455.1:p.Ile3286Met
XM_017009967.1:c.9843A>G	XP_016865456.1:p.Ile3281Met
XM_017009968.2:c.9939A>G	XP_016865457.1:p.Ile3313Met
XM_017009969.2:c.9939A>G	XP_016865458.1:p.Ile3313Met
XM_017009970.2:c.9939A>G	XP_016865459.1:p.Ile3313Met
XM_017009971.2:c.9939A>G	XP_016865460.1:p.Ile3313Met
XM_017009972.1:c.3057A>G	XP_016865461.1:p.Ile1019Met
XM_017009973.1:c.3036A>G	XP_016865462.1:p.Ile1012Met
XM_017009974.2:c.9939A>G	XP_016865463.1:p.Ile3313Met
XR_001742802.1:n.2523-9288T>C
XR_948560.1:n.272-9288T>C