Canonical Allele Identifier: CA360392078

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90781545A>G , CM000667.2:g.90781545A>G	GRCh38
NC_000005.9:g.90077362A>G , CM000667.1:g.90077362A>G	GRCh37
NC_000005.8:g.90113118A>G	NCBI36
NG_007083.1:g.227746A>G
NG_007083.2:g.257202A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.13198A>G MANE Select	NP_115495.3:p.Ile4400Val
ENST00000405460.9:c.13198A>G MANE Select	ENSP00000384582.2:p.Ile4400Val
NM_032119.3:c.13198A>G	NP_115495.3:p.Ile4400Val
NR_003149.1:n.13211A>G
NR_003149.2:n.13214A>G
ENST00000405460.6:c.13198A>G	ENSP00000384582.2:p.Ile4400Val
ENST00000425867.2:c.181A>G	ENSP00000392618.2:p.Ile61Val
ENST00000425867.3:c.2152A>G	ENSP00000392618.3:p.Ile718Val
ENST00000638510.1:n.465A>G
ENST00000639431.1:c.265+105336A>G	ENSP00000491057.1:n.265+105336A>G
XM_011543675.1:c.13195A>G	XP_011541977.1:p.Ile4399Val
XM_011543676.1:c.13117A>G	XP_011541978.1:p.Ile4373Val
XM_011543677.1:c.10501A>G	XP_011541979.1:p.Ile3501Val
XM_011543678.1:c.13198A>G	XP_011541980.1:p.Ile4400Val
XM_017009963.2:c.13219A>G	XP_016865452.1:p.Ile4407Val
XM_017009964.2:c.13216A>G	XP_016865453.1:p.Ile4406Val
XM_017009965.1:c.13216A>G	XP_016865454.1:p.Ile4406Val
XM_017009966.2:c.13138A>G	XP_016865455.1:p.Ile4380Val
XM_017009967.1:c.13123A>G	XP_016865456.1:p.Ile4375Val
XM_017009968.2:c.13219A>G	XP_016865457.1:p.Ile4407Val
XM_017009969.2:c.13219A>G	XP_016865458.1:p.Ile4407Val
XM_017009970.2:c.13219A>G	XP_016865459.1:p.Ile4407Val
XM_017009971.2:c.13219A>G	XP_016865460.1:p.Ile4407Val
XM_017009972.1:c.6337A>G	XP_016865461.1:p.Ile2113Val
XM_017009973.1:c.6316A>G	XP_016865462.1:p.Ile2106Val