Canonical Allele Identifier: CA360409089

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041485A>T (hg19) ; chr5:g.90745668A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745668A>T , CM000667.2:g.90745668A>T	GRCh38
NC_000005.9:g.90041485A>T , CM000667.1:g.90041485A>T	GRCh37
NC_000005.8:g.90077241A>T	NCBI36
NG_007083.1:g.191869A>T
NG_007083.2:g.221325A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10847A>T MANE Select	ENSP00000384582.2:p.Glu3616Val
ENST00000639431.1:c.265+69459A>T	ENSP00000491057.1:n.265+69459A>T
ENST00000640374.1:n.3991A>T
ENST00000640464.1:n.1266A>T
ENST00000405460.6:c.10847A>T	ENSP00000384582.2:p.Glu3616Val
ENST00000509621.1:c.3544A>T
NM_032119.3:c.10847A>T	NP_115495.3:p.Glu3616Val
NR_003149.1:n.10860A>T
XM_011543675.1:c.10844A>T	XP_011541977.1:p.Glu3615Val
XM_011543676.1:c.10766A>T	XP_011541978.1:p.Glu3589Val
XM_011543677.1:c.8150A>T	XP_011541979.1:p.Glu2717Val
XM_011543678.1:c.10847A>T	XP_011541980.1:p.Glu3616Val
XM_011543679.1:c.*69A>T	XP_011541981.1:n.*69A>T
NM_032119.4:c.10847A>T MANE Select	NP_115495.3:p.Glu3616Val
XM_017009963.2:c.10868A>T	XP_016865452.1:p.Glu3623Val
XM_017009964.2:c.10865A>T	XP_016865453.1:p.Glu3622Val
XM_017009965.1:c.10865A>T	XP_016865454.1:p.Glu3622Val
XM_017009966.2:c.10787A>T	XP_016865455.1:p.Glu3596Val
XM_017009967.1:c.10772A>T	XP_016865456.1:p.Glu3591Val
XM_017009968.2:c.10868A>T	XP_016865457.1:p.Glu3623Val
XM_017009969.2:c.10868A>T	XP_016865458.1:p.Glu3623Val
XM_017009970.2:c.10868A>T	XP_016865459.1:p.Glu3623Val
XM_017009971.2:c.10868A>T	XP_016865460.1:p.Glu3623Val
XM_017009972.1:c.3986A>T	XP_016865461.1:p.Glu1329Val
XM_017009973.1:c.3965A>T	XP_016865462.1:p.Glu1322Val
XM_017009974.2:c.*69A>T	XP_016865463.1:n.*69A>T
NR_003149.2:n.10863A>T