Canonical Allele Identifier: CA360396232

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008156T>A (hg19) ; chr5:g.90712339T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712339T>A , CM000667.2:g.90712339T>A	GRCh38
NC_000005.9:g.90008156T>A , CM000667.1:g.90008156T>A	GRCh37
NC_000005.8:g.90043912T>A	NCBI36
NG_007083.1:g.158540T>A
NG_007083.2:g.187996T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9095T>A MANE Select	ENSP00000384582.2:p.Leu3032His
ENST00000639431.1:c.265+36130T>A	ENSP00000491057.1:n.265+36130T>A
ENST00000639473.1:n.4554T>A
ENST00000640012.1:c.2902T>A
ENST00000640374.1:n.2239T>A
ENST00000640779.1:c.3824T>A
ENST00000405460.6:c.9095T>A	ENSP00000384582.2:p.Leu3032His
ENST00000509621.1:c.1792T>A
NM_032119.3:c.9095T>A	NP_115495.3:p.Leu3032His
NR_003149.1:n.9108T>A
XM_011543675.1:c.9092T>A	XP_011541977.1:p.Leu3031His
XM_011543676.1:c.9014T>A	XP_011541978.1:p.Leu3005His
XM_011543677.1:c.6398T>A	XP_011541979.1:p.Leu2133His
XM_011543678.1:c.9095T>A	XP_011541980.1:p.Leu3032His
XM_011543679.1:c.9095T>A	XP_011541981.1:p.Leu3032His
NM_032119.4:c.9095T>A MANE Select	NP_115495.3:p.Leu3032His
XM_017009963.2:c.9116T>A	XP_016865452.1:p.Leu3039His
XM_017009964.2:c.9113T>A	XP_016865453.1:p.Leu3038His
XM_017009965.1:c.9113T>A	XP_016865454.1:p.Leu3038His
XM_017009966.2:c.9035T>A	XP_016865455.1:p.Leu3012His
XM_017009967.1:c.9020T>A	XP_016865456.1:p.Leu3007His
XM_017009968.2:c.9116T>A	XP_016865457.1:p.Leu3039His
XM_017009969.2:c.9116T>A	XP_016865458.1:p.Leu3039His
XM_017009970.2:c.9116T>A	XP_016865459.1:p.Leu3039His
XM_017009971.2:c.9116T>A	XP_016865460.1:p.Leu3039His
XM_017009972.1:c.2234T>A	XP_016865461.1:p.Leu745His
XM_017009973.1:c.2213T>A	XP_016865462.1:p.Leu738His
XM_017009974.2:c.9116T>A	XP_016865463.1:p.Leu3039His
NR_003149.2:n.9111T>A