Canonical Allele Identifier: CA360409016

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041467T>G (hg19) ; chr5:g.90745650T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745650T>G , CM000667.2:g.90745650T>G	GRCh38
NC_000005.9:g.90041467T>G , CM000667.1:g.90041467T>G	GRCh37
NC_000005.8:g.90077223T>G	NCBI36
NG_007083.1:g.191851T>G
NG_007083.2:g.221307T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10829T>G MANE Select	ENSP00000384582.2:p.Leu3610Arg
ENST00000639431.1:c.265+69441T>G	ENSP00000491057.1:n.265+69441T>G
ENST00000640374.1:n.3973T>G
ENST00000640464.1:n.1248T>G
ENST00000405460.6:c.10829T>G	ENSP00000384582.2:p.Leu3610Arg
ENST00000509621.1:c.3526T>G
NM_032119.3:c.10829T>G	NP_115495.3:p.Leu3610Arg
NR_003149.1:n.10842T>G
XM_011543675.1:c.10826T>G	XP_011541977.1:p.Leu3609Arg
XM_011543676.1:c.10748T>G	XP_011541978.1:p.Leu3583Arg
XM_011543677.1:c.8132T>G	XP_011541979.1:p.Leu2711Arg
XM_011543678.1:c.10829T>G	XP_011541980.1:p.Leu3610Arg
XM_011543679.1:c.*51T>G	XP_011541981.1:n.*51T>G
NM_032119.4:c.10829T>G MANE Select	NP_115495.3:p.Leu3610Arg
XM_017009963.2:c.10850T>G	XP_016865452.1:p.Leu3617Arg
XM_017009964.2:c.10847T>G	XP_016865453.1:p.Leu3616Arg
XM_017009965.1:c.10847T>G	XP_016865454.1:p.Leu3616Arg
XM_017009966.2:c.10769T>G	XP_016865455.1:p.Leu3590Arg
XM_017009967.1:c.10754T>G	XP_016865456.1:p.Leu3585Arg
XM_017009968.2:c.10850T>G	XP_016865457.1:p.Leu3617Arg
XM_017009969.2:c.10850T>G	XP_016865458.1:p.Leu3617Arg
XM_017009970.2:c.10850T>G	XP_016865459.1:p.Leu3617Arg
XM_017009971.2:c.10850T>G	XP_016865460.1:p.Leu3617Arg
XM_017009972.1:c.3968T>G	XP_016865461.1:p.Leu1323Arg
XM_017009973.1:c.3947T>G	XP_016865462.1:p.Leu1316Arg
XM_017009974.2:c.*51T>G	XP_016865463.1:n.*51T>G
NR_003149.2:n.10845T>G