Canonical Allele Identifier: CA3342595

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.91072511G>A , CM000667.2:g.91072511G>A	GRCh38
NC_000005.9:g.90368328G>A , CM000667.1:g.90368328G>A	GRCh37
NC_000005.8:g.90404084G>A	NCBI36
NG_007083.1:g.518712G>A
NG_007083.2:g.548168G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.18217G>A MANE Select	NP_115495.3:p.Val6073Met
ENST00000405460.9:c.18217G>A MANE Select	ENSP00000384582.2:p.Val6073Met
NM_032119.3:c.18217G>A	NP_115495.3:p.Val6073Met
NR_003149.1:n.18230G>A
NR_003149.2:n.18233G>A
ENST00000405460.6:c.18217G>A	ENSP00000384582.2:p.Val6073Met
ENST00000425867.2:c.5200G>A	ENSP00000392618.2:p.Val1734Met
ENST00000425867.3:c.7171G>A	ENSP00000392618.3:p.Val2391Met
ENST00000638510.1:n.5484G>A
ENST00000638990.1:c.1429G>A
ENST00000639431.1:c.509G>A	ENSP00000491057.1:n.509G>A
ENST00000639707.1:c.301G>A	ENSP00000492328.1:p.Val101Met
ENST00000639821.1:c.301G>A	ENSP00000492216.1:p.Val101Met
ENST00000640369.1:c.301G>A	ENSP00000491401.1:p.Val101Met
ENST00000640407.1:c.4666G>A	ENSP00000491425.1:n.4666G>A
ENST00000640815.1:c.301G>A	ENSP00000491767.1:p.Val101Met
XM_011543675.1:c.18214G>A	XP_011541977.1:p.Val6072Met
XM_011543676.1:c.18136G>A	XP_011541978.1:p.Val6046Met
XM_011543677.1:c.15520G>A	XP_011541979.1:p.Val5174Met
XM_017009963.2:c.18238G>A	XP_016865452.1:p.Val6080Met
XM_017009964.2:c.18235G>A	XP_016865453.1:p.Val6079Met
XM_017009965.1:c.18235G>A	XP_016865454.1:p.Val6079Met
XM_017009966.2:c.18157G>A	XP_016865455.1:p.Val6053Met
XM_017009967.1:c.18142G>A	XP_016865456.1:p.Val6048Met
XM_017009968.2:c.18058G>A	XP_016865457.1:p.Val6020Met
XM_017009969.2:c.18238G>A	XP_016865458.1:p.Val6080Met
XM_017009972.1:c.11356G>A	XP_016865461.1:p.Val3786Met
XM_017009973.1:c.11335G>A	XP_016865462.1:p.Val3779Met