Canonical Allele Identifier: CA360377388

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059160T>A (hg19) ; chr5:g.90763343T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763343T>A , CM000667.2:g.90763343T>A	GRCh38
NC_000005.9:g.90059160T>A , CM000667.1:g.90059160T>A	GRCh37
NC_000005.8:g.90094916T>A	NCBI36
NG_007083.1:g.209544T>A
NG_007083.2:g.239000T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12159T>A MANE Select	ENSP00000384582.2:p.Asp4053Glu
ENST00000425867.3:c.1113T>A	ENSP00000392618.3:p.Asp371Glu
ENST00000639431.1:c.265+87134T>A	ENSP00000491057.1:n.265+87134T>A
ENST00000640464.1:n.2578T>A
ENST00000640729.1:n.736T>A
ENST00000405460.6:c.12159T>A	ENSP00000384582.2:p.Asp4053Glu
NM_032119.3:c.12159T>A	NP_115495.3:p.Asp4053Glu
NR_003149.1:n.12172T>A
XM_011543675.1:c.12156T>A	XP_011541977.1:p.Asp4052Glu
XM_011543676.1:c.12078T>A	XP_011541978.1:p.Asp4026Glu
XM_011543677.1:c.9462T>A	XP_011541979.1:p.Asp3154Glu
XM_011543678.1:c.12159T>A	XP_011541980.1:p.Asp4053Glu
NM_032119.4:c.12159T>A MANE Select	NP_115495.3:p.Asp4053Glu
XM_017009963.2:c.12180T>A	XP_016865452.1:p.Asp4060Glu
XM_017009964.2:c.12177T>A	XP_016865453.1:p.Asp4059Glu
XM_017009965.1:c.12177T>A	XP_016865454.1:p.Asp4059Glu
XM_017009966.2:c.12099T>A	XP_016865455.1:p.Asp4033Glu
XM_017009967.1:c.12084T>A	XP_016865456.1:p.Asp4028Glu
XM_017009968.2:c.12180T>A	XP_016865457.1:p.Asp4060Glu
XM_017009969.2:c.12180T>A	XP_016865458.1:p.Asp4060Glu
XM_017009970.2:c.12180T>A	XP_016865459.1:p.Asp4060Glu
XM_017009971.2:c.12180T>A	XP_016865460.1:p.Asp4060Glu
XM_017009972.1:c.5298T>A	XP_016865461.1:p.Asp1766Glu
XM_017009973.1:c.5277T>A	XP_016865462.1:p.Asp1759Glu
NR_003149.2:n.12175T>A