Canonical Allele Identifier: CA360409188

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041506T>G (hg19) ; chr5:g.90745689T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745689T>G , CM000667.2:g.90745689T>G	GRCh38
NC_000005.9:g.90041506T>G , CM000667.1:g.90041506T>G	GRCh37
NC_000005.8:g.90077262T>G	NCBI36
NG_007083.1:g.191890T>G
NG_007083.2:g.221346T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10868T>G MANE Select	ENSP00000384582.2:p.Val3623Gly
ENST00000639431.1:c.265+69480T>G	ENSP00000491057.1:n.265+69480T>G
ENST00000640374.1:n.4012T>G
ENST00000640464.1:n.1287T>G
ENST00000405460.6:c.10868T>G	ENSP00000384582.2:p.Val3623Gly
ENST00000509621.1:c.3565T>G
NM_032119.3:c.10868T>G	NP_115495.3:p.Val3623Gly
NR_003149.1:n.10881T>G
XM_011543675.1:c.10865T>G	XP_011541977.1:p.Val3622Gly
XM_011543676.1:c.10787T>G	XP_011541978.1:p.Val3596Gly
XM_011543677.1:c.8171T>G	XP_011541979.1:p.Val2724Gly
XM_011543678.1:c.10868T>G	XP_011541980.1:p.Val3623Gly
NM_032119.4:c.10868T>G MANE Select	NP_115495.3:p.Val3623Gly
XM_017009963.2:c.10889T>G	XP_016865452.1:p.Val3630Gly
XM_017009964.2:c.10886T>G	XP_016865453.1:p.Val3629Gly
XM_017009965.1:c.10886T>G	XP_016865454.1:p.Val3629Gly
XM_017009966.2:c.10808T>G	XP_016865455.1:p.Val3603Gly
XM_017009967.1:c.10793T>G	XP_016865456.1:p.Val3598Gly
XM_017009968.2:c.10889T>G	XP_016865457.1:p.Val3630Gly
XM_017009969.2:c.10889T>G	XP_016865458.1:p.Val3630Gly
XM_017009970.2:c.10889T>G	XP_016865459.1:p.Val3630Gly
XM_017009971.2:c.10889T>G	XP_016865460.1:p.Val3630Gly
XM_017009972.1:c.4007T>G	XP_016865461.1:p.Val1336Gly
XM_017009973.1:c.3986T>G	XP_016865462.1:p.Val1329Gly
NR_003149.2:n.10884T>G