Canonical Allele Identifier: CA360401281

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086925C>A (hg19) ; chr5:g.90791108C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791108C>A , CM000667.2:g.90791108C>A	GRCh38
NC_000005.9:g.90086925C>A , CM000667.1:g.90086925C>A	GRCh37
NC_000005.8:g.90122681C>A	NCBI36
NG_007083.1:g.237309C>A
NG_007083.2:g.266765C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14279C>A MANE Select	ENSP00000384582.2:p.Pro4760Gln
ENST00000425867.3:c.3233C>A	ENSP00000392618.3:p.Pro1078Gln
ENST00000638510.1:n.1546C>A
ENST00000638585.1:n.45C>A
ENST00000638975.1:c.908C>A	ENSP00000492630.1:p.Pro303Gln
ENST00000639431.1:c.265+114899C>A	ENSP00000491057.1:n.265+114899C>A
ENST00000640407.1:c.689C>A	ENSP00000491425.1:p.Pro230Gln
ENST00000405460.6:c.14279C>A	ENSP00000384582.2:p.Pro4760Gln
ENST00000425867.2:c.1262C>A	ENSP00000392618.2:p.Pro421Gln
NM_032119.3:c.14279C>A	NP_115495.3:p.Pro4760Gln
NR_003149.1:n.14292C>A
XM_011543675.1:c.14276C>A	XP_011541977.1:p.Pro4759Gln
XM_011543676.1:c.14198C>A	XP_011541978.1:p.Pro4733Gln
XM_011543677.1:c.11582C>A	XP_011541979.1:p.Pro3861Gln
XM_011543678.1:c.14279C>A	XP_011541980.1:p.Pro4760Gln
NM_032119.4:c.14279C>A MANE Select	NP_115495.3:p.Pro4760Gln
XM_017009963.2:c.14300C>A	XP_016865452.1:p.Pro4767Gln
XM_017009964.2:c.14297C>A	XP_016865453.1:p.Pro4766Gln
XM_017009965.1:c.14297C>A	XP_016865454.1:p.Pro4766Gln
XM_017009966.2:c.14219C>A	XP_016865455.1:p.Pro4740Gln
XM_017009967.1:c.14204C>A	XP_016865456.1:p.Pro4735Gln
XM_017009968.2:c.14300C>A	XP_016865457.1:p.Pro4767Gln
XM_017009969.2:c.14300C>A	XP_016865458.1:p.Pro4767Gln
XM_017009970.2:c.14300C>A	XP_016865459.1:p.Pro4767Gln
XM_017009971.2:c.14300C>A	XP_016865460.1:p.Pro4767Gln
XM_017009972.1:c.7418C>A	XP_016865461.1:p.Pro2473Gln
XM_017009973.1:c.7397C>A	XP_016865462.1:p.Pro2466Gln
NR_003149.2:n.14295C>A