Canonical Allele Identifier: CA360396119

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008107C>G (hg19) ; chr5:g.90712290C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712290C>G , CM000667.2:g.90712290C>G	GRCh38
NC_000005.9:g.90008107C>G , CM000667.1:g.90008107C>G	GRCh37
NC_000005.8:g.90043863C>G	NCBI36
NG_007083.1:g.158491C>G
NG_007083.2:g.187947C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9046C>G MANE Select	ENSP00000384582.2:p.Leu3016Val
ENST00000639431.1:c.265+36081C>G	ENSP00000491057.1:n.265+36081C>G
ENST00000639473.1:n.4505C>G
ENST00000640012.1:c.2853C>G
ENST00000640374.1:n.2190C>G
ENST00000640779.1:c.3775C>G
ENST00000405460.6:c.9046C>G	ENSP00000384582.2:p.Leu3016Val
ENST00000509621.1:c.1743C>G
NM_032119.3:c.9046C>G	NP_115495.3:p.Leu3016Val
NR_003149.1:n.9059C>G
XM_011543675.1:c.9043C>G	XP_011541977.1:p.Leu3015Val
XM_011543676.1:c.8965C>G	XP_011541978.1:p.Leu2989Val
XM_011543677.1:c.6349C>G	XP_011541979.1:p.Leu2117Val
XM_011543678.1:c.9046C>G	XP_011541980.1:p.Leu3016Val
XM_011543679.1:c.9046C>G	XP_011541981.1:p.Leu3016Val
NM_032119.4:c.9046C>G MANE Select	NP_115495.3:p.Leu3016Val
XM_017009963.2:c.9067C>G	XP_016865452.1:p.Leu3023Val
XM_017009964.2:c.9064C>G	XP_016865453.1:p.Leu3022Val
XM_017009965.1:c.9064C>G	XP_016865454.1:p.Leu3022Val
XM_017009966.2:c.8986C>G	XP_016865455.1:p.Leu2996Val
XM_017009967.1:c.8971C>G	XP_016865456.1:p.Leu2991Val
XM_017009968.2:c.9067C>G	XP_016865457.1:p.Leu3023Val
XM_017009969.2:c.9067C>G	XP_016865458.1:p.Leu3023Val
XM_017009970.2:c.9067C>G	XP_016865459.1:p.Leu3023Val
XM_017009971.2:c.9067C>G	XP_016865460.1:p.Leu3023Val
XM_017009972.1:c.2185C>G	XP_016865461.1:p.Leu729Val
XM_017009973.1:c.2164C>G	XP_016865462.1:p.Leu722Val
XM_017009974.2:c.9067C>G	XP_016865463.1:p.Leu3023Val
NR_003149.2:n.9062C>G