Canonical Allele Identifier: CA360403209

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90021388A>T (hg19) ; chr5:g.90725571A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90725571A>T , CM000667.2:g.90725571A>T	GRCh38
NC_000005.9:g.90021388A>T , CM000667.1:g.90021388A>T	GRCh37
NC_000005.8:g.90057144A>T	NCBI36
NG_007083.1:g.171772A>T
NG_007083.2:g.201228A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10076A>T MANE Select	ENSP00000384582.2:p.Glu3359Val
ENST00000639431.1:c.265+49362A>T	ENSP00000491057.1:n.265+49362A>T
ENST00000640374.1:n.3220A>T
ENST00000640464.1:n.495A>T
ENST00000405460.6:c.10076A>T	ENSP00000384582.2:p.Glu3359Val
ENST00000509621.1:c.2773A>T
NM_032119.3:c.10076A>T	NP_115495.3:p.Glu3359Val
NR_003149.1:n.10089A>T
XM_011543675.1:c.10073A>T	XP_011541977.1:p.Glu3358Val
XM_011543676.1:c.9995A>T	XP_011541978.1:p.Glu3332Val
XM_011543677.1:c.7379A>T	XP_011541979.1:p.Glu2460Val
XM_011543678.1:c.10076A>T	XP_011541980.1:p.Glu3359Val
XM_011543679.1:c.10076A>T	XP_011541981.1:p.Glu3359Val
XR_948560.1:n.272-9762T>A
NM_032119.4:c.10076A>T MANE Select	NP_115495.3:p.Glu3359Val
XM_017009963.2:c.10097A>T	XP_016865452.1:p.Glu3366Val
XM_017009964.2:c.10094A>T	XP_016865453.1:p.Glu3365Val
XM_017009965.1:c.10094A>T	XP_016865454.1:p.Glu3365Val
XM_017009966.2:c.10016A>T	XP_016865455.1:p.Glu3339Val
XM_017009967.1:c.10001A>T	XP_016865456.1:p.Glu3334Val
XM_017009968.2:c.10097A>T	XP_016865457.1:p.Glu3366Val
XM_017009969.2:c.10097A>T	XP_016865458.1:p.Glu3366Val
XM_017009970.2:c.10097A>T	XP_016865459.1:p.Glu3366Val
XM_017009971.2:c.10097A>T	XP_016865460.1:p.Glu3366Val
XM_017009972.1:c.3215A>T	XP_016865461.1:p.Glu1072Val
XM_017009973.1:c.3194A>T	XP_016865462.1:p.Glu1065Val
XM_017009974.2:c.10097A>T	XP_016865463.1:p.Glu3366Val
XR_001742802.1:n.2523-9762T>A
NR_003149.2:n.10092A>T