Canonical Allele Identifier: CA360401742

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90087035G>A (hg19) ; chr5:g.90791218G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791218G>A , CM000667.2:g.90791218G>A	GRCh38
NC_000005.9:g.90087035G>A , CM000667.1:g.90087035G>A	GRCh37
NC_000005.8:g.90122791G>A	NCBI36
NG_007083.1:g.237419G>A
NG_007083.2:g.266875G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14389G>A MANE Select	ENSP00000384582.2:p.Val4797Met
ENST00000425867.3:c.3343G>A	ENSP00000392618.3:p.Val1115Met
ENST00000507314.2:c.64G>A	ENSP00000491299.1:p.Val22Met
ENST00000638510.1:n.1656G>A
ENST00000638585.1:n.155G>A
ENST00000638975.1:c.1018G>A	ENSP00000492630.1:p.Val340Met
ENST00000639431.1:c.265+115009G>A	ENSP00000491057.1:n.265+115009G>A
ENST00000640407.1:c.799G>A	ENSP00000491425.1:p.Val267Met
ENST00000405460.6:c.14389G>A	ENSP00000384582.2:p.Val4797Met
ENST00000425867.2:c.1372G>A	ENSP00000392618.2:p.Val458Met
ENST00000507314.1:n.64G>A
NM_032119.3:c.14389G>A	NP_115495.3:p.Val4797Met
NR_003149.1:n.14402G>A
XM_011543675.1:c.14386G>A	XP_011541977.1:p.Val4796Met
XM_011543676.1:c.14308G>A	XP_011541978.1:p.Val4770Met
XM_011543677.1:c.11692G>A	XP_011541979.1:p.Val3898Met
XM_011543678.1:c.14389G>A	XP_011541980.1:p.Val4797Met
NM_032119.4:c.14389G>A MANE Select	NP_115495.3:p.Val4797Met
XM_017009963.2:c.14410G>A	XP_016865452.1:p.Val4804Met
XM_017009964.2:c.14407G>A	XP_016865453.1:p.Val4803Met
XM_017009965.1:c.14407G>A	XP_016865454.1:p.Val4803Met
XM_017009966.2:c.14329G>A	XP_016865455.1:p.Val4777Met
XM_017009967.1:c.14314G>A	XP_016865456.1:p.Val4772Met
XM_017009968.2:c.14410G>A	XP_016865457.1:p.Val4804Met
XM_017009969.2:c.14410G>A	XP_016865458.1:p.Val4804Met
XM_017009970.2:c.14410G>A	XP_016865459.1:p.Val4804Met
XM_017009971.2:c.14410G>A	XP_016865460.1:p.Val4804Met
XM_017009972.1:c.7528G>A	XP_016865461.1:p.Val2510Met
XM_017009973.1:c.7507G>A	XP_016865462.1:p.Val2503Met
NR_003149.2:n.14405G>A