Canonical Allele Identifier: CA360397788

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012532G>T (hg19) ; chr5:g.90716715G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716715G>T , CM000667.2:g.90716715G>T	GRCh38
NC_000005.9:g.90012532G>T , CM000667.1:g.90012532G>T	GRCh37
NC_000005.8:g.90048288G>T	NCBI36
NG_007083.1:g.162916G>T
NG_007083.2:g.192372G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9433G>T MANE Select	ENSP00000384582.2:p.Gly3145Cys
ENST00000639431.1:c.265+40506G>T	ENSP00000491057.1:n.265+40506G>T
ENST00000639473.1:n.4892G>T
ENST00000640012.1:c.3240G>T
ENST00000640374.1:n.2577G>T
ENST00000640779.1:c.4162G>T
ENST00000405460.6:c.9433G>T	ENSP00000384582.2:p.Gly3145Cys
ENST00000509621.1:c.2130G>T
NM_032119.3:c.9433G>T	NP_115495.3:p.Gly3145Cys
NR_003149.1:n.9446G>T
XM_011543675.1:c.9430G>T	XP_011541977.1:p.Gly3144Cys
XM_011543676.1:c.9352G>T	XP_011541978.1:p.Gly3118Cys
XM_011543677.1:c.6736G>T	XP_011541979.1:p.Gly2246Cys
XM_011543678.1:c.9433G>T	XP_011541980.1:p.Gly3145Cys
XM_011543679.1:c.9433G>T	XP_011541981.1:p.Gly3145Cys
XR_948560.1:n.272-906C>A
NM_032119.4:c.9433G>T MANE Select	NP_115495.3:p.Gly3145Cys
XM_017009963.2:c.9454G>T	XP_016865452.1:p.Gly3152Cys
XM_017009964.2:c.9451G>T	XP_016865453.1:p.Gly3151Cys
XM_017009965.1:c.9451G>T	XP_016865454.1:p.Gly3151Cys
XM_017009966.2:c.9373G>T	XP_016865455.1:p.Gly3125Cys
XM_017009967.1:c.9358G>T	XP_016865456.1:p.Gly3120Cys
XM_017009968.2:c.9454G>T	XP_016865457.1:p.Gly3152Cys
XM_017009969.2:c.9454G>T	XP_016865458.1:p.Gly3152Cys
XM_017009970.2:c.9454G>T	XP_016865459.1:p.Gly3152Cys
XM_017009971.2:c.9454G>T	XP_016865460.1:p.Gly3152Cys
XM_017009972.1:c.2572G>T	XP_016865461.1:p.Gly858Cys
XM_017009973.1:c.2551G>T	XP_016865462.1:p.Gly851Cys
XM_017009974.2:c.9454G>T	XP_016865463.1:p.Gly3152Cys
XR_001742802.1:n.2523-906C>A
NR_003149.2:n.9449G>T