Canonical Allele Identifier: CA360409178

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041505G>A (hg19) ; chr5:g.90745688G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745688G>A , CM000667.2:g.90745688G>A	GRCh38
NC_000005.9:g.90041505G>A , CM000667.1:g.90041505G>A	GRCh37
NC_000005.8:g.90077261G>A	NCBI36
NG_007083.1:g.191889G>A
NG_007083.2:g.221345G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10867G>A MANE Select	ENSP00000384582.2:p.Val3623Ile
ENST00000639431.1:c.265+69479G>A	ENSP00000491057.1:n.265+69479G>A
ENST00000640374.1:n.4011G>A
ENST00000640464.1:n.1286G>A
ENST00000405460.6:c.10867G>A	ENSP00000384582.2:p.Val3623Ile
ENST00000509621.1:c.3564G>A
NM_032119.3:c.10867G>A	NP_115495.3:p.Val3623Ile
NR_003149.1:n.10880G>A
XM_011543675.1:c.10864G>A	XP_011541977.1:p.Val3622Ile
XM_011543676.1:c.10786G>A	XP_011541978.1:p.Val3596Ile
XM_011543677.1:c.8170G>A	XP_011541979.1:p.Val2724Ile
XM_011543678.1:c.10867G>A	XP_011541980.1:p.Val3623Ile
NM_032119.4:c.10867G>A MANE Select	NP_115495.3:p.Val3623Ile
XM_017009963.2:c.10888G>A	XP_016865452.1:p.Val3630Ile
XM_017009964.2:c.10885G>A	XP_016865453.1:p.Val3629Ile
XM_017009965.1:c.10885G>A	XP_016865454.1:p.Val3629Ile
XM_017009966.2:c.10807G>A	XP_016865455.1:p.Val3603Ile
XM_017009967.1:c.10792G>A	XP_016865456.1:p.Val3598Ile
XM_017009968.2:c.10888G>A	XP_016865457.1:p.Val3630Ile
XM_017009969.2:c.10888G>A	XP_016865458.1:p.Val3630Ile
XM_017009970.2:c.10888G>A	XP_016865459.1:p.Val3630Ile
XM_017009971.2:c.10888G>A	XP_016865460.1:p.Val3630Ile
XM_017009972.1:c.4006G>A	XP_016865461.1:p.Val1336Ile
XM_017009973.1:c.3985G>A	XP_016865462.1:p.Val1329Ile
NR_003149.2:n.10883G>A