Canonical Allele Identifier: CA360377077

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90059129T>G (hg19) ; chr5:g.90763312T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763312T>G , CM000667.2:g.90763312T>G	GRCh38
NC_000005.9:g.90059129T>G , CM000667.1:g.90059129T>G	GRCh37
NC_000005.8:g.90094885T>G	NCBI36
NG_007083.1:g.209513T>G
NG_007083.2:g.238969T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12128T>G MANE Select	ENSP00000384582.2:p.Ile4043Ser
ENST00000425867.3:c.1082T>G	ENSP00000392618.3:p.Ile361Ser
ENST00000639431.1:c.265+87103T>G	ENSP00000491057.1:n.265+87103T>G
ENST00000640464.1:n.2547T>G
ENST00000640729.1:n.705T>G
ENST00000405460.6:c.12128T>G	ENSP00000384582.2:p.Ile4043Ser
NM_032119.3:c.12128T>G	NP_115495.3:p.Ile4043Ser
NR_003149.1:n.12141T>G
XM_011543675.1:c.12125T>G	XP_011541977.1:p.Ile4042Ser
XM_011543676.1:c.12047T>G	XP_011541978.1:p.Ile4016Ser
XM_011543677.1:c.9431T>G	XP_011541979.1:p.Ile3144Ser
XM_011543678.1:c.12128T>G	XP_011541980.1:p.Ile4043Ser
NM_032119.4:c.12128T>G MANE Select	NP_115495.3:p.Ile4043Ser
XM_017009963.2:c.12149T>G	XP_016865452.1:p.Ile4050Ser
XM_017009964.2:c.12146T>G	XP_016865453.1:p.Ile4049Ser
XM_017009965.1:c.12146T>G	XP_016865454.1:p.Ile4049Ser
XM_017009966.2:c.12068T>G	XP_016865455.1:p.Ile4023Ser
XM_017009967.1:c.12053T>G	XP_016865456.1:p.Ile4018Ser
XM_017009968.2:c.12149T>G	XP_016865457.1:p.Ile4050Ser
XM_017009969.2:c.12149T>G	XP_016865458.1:p.Ile4050Ser
XM_017009970.2:c.12149T>G	XP_016865459.1:p.Ile4050Ser
XM_017009971.2:c.12149T>G	XP_016865460.1:p.Ile4050Ser
XM_017009972.1:c.5267T>G	XP_016865461.1:p.Ile1756Ser
XM_017009973.1:c.5246T>G	XP_016865462.1:p.Ile1749Ser
NR_003149.2:n.12144T>G