Canonical Allele Identifier: CA360408791

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1754531788
• MyVariant Identifiers: chr5:g.90041415G>A (hg19) ; chr5:g.90745598G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745598G>A , CM000667.2:g.90745598G>A	GRCh38
NC_000005.9:g.90041415G>A , CM000667.1:g.90041415G>A	GRCh37
NC_000005.8:g.90077171G>A	NCBI36
NG_007083.1:g.191799G>A
NG_007083.2:g.221255G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10777G>A MANE Select	ENSP00000384582.2:p.Glu3593Lys
ENST00000639431.1:c.265+69389G>A	ENSP00000491057.1:n.265+69389G>A
ENST00000640374.1:n.3921G>A
ENST00000640464.1:n.1196G>A
ENST00000405460.6:c.10777G>A	ENSP00000384582.2:p.Glu3593Lys
ENST00000509621.1:c.3474G>A
NM_032119.3:c.10777G>A	NP_115495.3:p.Glu3593Lys
NR_003149.1:n.10790G>A
XM_011543675.1:c.10774G>A	XP_011541977.1:p.Glu3592Lys
XM_011543676.1:c.10696G>A	XP_011541978.1:p.Glu3566Lys
XM_011543677.1:c.8080G>A	XP_011541979.1:p.Glu2694Lys
XM_011543678.1:c.10777G>A	XP_011541980.1:p.Glu3593Lys
XM_011543679.1:c.10772G>A	XP_011541981.1:p.Ter3591=
NM_032119.4:c.10777G>A MANE Select	NP_115495.3:p.Glu3593Lys
XM_017009963.2:c.10798G>A	XP_016865452.1:p.Glu3600Lys
XM_017009964.2:c.10795G>A	XP_016865453.1:p.Glu3599Lys
XM_017009965.1:c.10795G>A	XP_016865454.1:p.Glu3599Lys
XM_017009966.2:c.10717G>A	XP_016865455.1:p.Glu3573Lys
XM_017009967.1:c.10702G>A	XP_016865456.1:p.Glu3568Lys
XM_017009968.2:c.10798G>A	XP_016865457.1:p.Glu3600Lys
XM_017009969.2:c.10798G>A	XP_016865458.1:p.Glu3600Lys
XM_017009970.2:c.10798G>A	XP_016865459.1:p.Glu3600Lys
XM_017009971.2:c.10798G>A	XP_016865460.1:p.Glu3600Lys
XM_017009972.1:c.3916G>A	XP_016865461.1:p.Glu1306Lys
XM_017009973.1:c.3895G>A	XP_016865462.1:p.Glu1299Lys
XM_017009974.2:c.10793G>A	XP_016865463.1:p.Ter3598=
NR_003149.2:n.10793G>A