Canonical Allele Identifier: CA360396123

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008108T>G (hg19) ; chr5:g.90712291T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712291T>G , CM000667.2:g.90712291T>G	GRCh38
NC_000005.9:g.90008108T>G , CM000667.1:g.90008108T>G	GRCh37
NC_000005.8:g.90043864T>G	NCBI36
NG_007083.1:g.158492T>G
NG_007083.2:g.187948T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9047T>G MANE Select	ENSP00000384582.2:p.Leu3016Arg
ENST00000639431.1:c.265+36082T>G	ENSP00000491057.1:n.265+36082T>G
ENST00000639473.1:n.4506T>G
ENST00000640012.1:c.2854T>G
ENST00000640374.1:n.2191T>G
ENST00000640779.1:c.3776T>G
ENST00000405460.6:c.9047T>G	ENSP00000384582.2:p.Leu3016Arg
ENST00000509621.1:c.1744T>G
NM_032119.3:c.9047T>G	NP_115495.3:p.Leu3016Arg
NR_003149.1:n.9060T>G
XM_011543675.1:c.9044T>G	XP_011541977.1:p.Leu3015Arg
XM_011543676.1:c.8966T>G	XP_011541978.1:p.Leu2989Arg
XM_011543677.1:c.6350T>G	XP_011541979.1:p.Leu2117Arg
XM_011543678.1:c.9047T>G	XP_011541980.1:p.Leu3016Arg
XM_011543679.1:c.9047T>G	XP_011541981.1:p.Leu3016Arg
NM_032119.4:c.9047T>G MANE Select	NP_115495.3:p.Leu3016Arg
XM_017009963.2:c.9068T>G	XP_016865452.1:p.Leu3023Arg
XM_017009964.2:c.9065T>G	XP_016865453.1:p.Leu3022Arg
XM_017009965.1:c.9065T>G	XP_016865454.1:p.Leu3022Arg
XM_017009966.2:c.8987T>G	XP_016865455.1:p.Leu2996Arg
XM_017009967.1:c.8972T>G	XP_016865456.1:p.Leu2991Arg
XM_017009968.2:c.9068T>G	XP_016865457.1:p.Leu3023Arg
XM_017009969.2:c.9068T>G	XP_016865458.1:p.Leu3023Arg
XM_017009970.2:c.9068T>G	XP_016865459.1:p.Leu3023Arg
XM_017009971.2:c.9068T>G	XP_016865460.1:p.Leu3023Arg
XM_017009972.1:c.2186T>G	XP_016865461.1:p.Leu729Arg
XM_017009973.1:c.2165T>G	XP_016865462.1:p.Leu722Arg
XM_017009974.2:c.9068T>G	XP_016865463.1:p.Leu3023Arg
NR_003149.2:n.9063T>G