Canonical Allele Identifier: CA445467515

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086926A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791109A>G , CM000667.2:g.90791109A>G	GRCh38
NC_000005.9:g.90086926A>G , CM000667.1:g.90086926A>G	GRCh37
NC_000005.8:g.90122682A>G	NCBI36
NG_007083.1:g.237310A>G
NG_007083.2:g.266766A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.14280A>G MANE Select	ENSP00000384582.2:p.Pro4760=
ENST00000425867.3:c.3234A>G	ENSP00000392618.3:p.Pro1078=
ENST00000638510.1:n.1547A>G
ENST00000638585.1:n.46A>G
ENST00000638975.1:c.909A>G	ENSP00000492630.1:p.Pro303=
ENST00000639431.1:c.265+114900A>G	ENSP00000491057.1:n.265+114900A>G
ENST00000640407.1:c.690A>G	ENSP00000491425.1:p.Pro230=
ENST00000405460.6:c.14280A>G	ENSP00000384582.2:p.Pro4760=
ENST00000425867.2:c.1263A>G	ENSP00000392618.2:p.Pro421=
NM_032119.3:c.14280A>G	NP_115495.3:p.Pro4760=
NR_003149.1:n.14293A>G
XM_011543675.1:c.14277A>G	XP_011541977.1:p.Pro4759=
XM_011543676.1:c.14199A>G	XP_011541978.1:p.Pro4733=
XM_011543677.1:c.11583A>G	XP_011541979.1:p.Pro3861=
XM_011543678.1:c.14280A>G	XP_011541980.1:p.Pro4760=
NM_032119.4:c.14280A>G MANE Select	NP_115495.3:p.Pro4760=
XM_017009963.2:c.14301A>G	XP_016865452.1:p.Pro4767=
XM_017009964.2:c.14298A>G	XP_016865453.1:p.Pro4766=
XM_017009965.1:c.14298A>G	XP_016865454.1:p.Pro4766=
XM_017009966.2:c.14220A>G	XP_016865455.1:p.Pro4740=
XM_017009967.1:c.14205A>G	XP_016865456.1:p.Pro4735=
XM_017009968.2:c.14301A>G	XP_016865457.1:p.Pro4767=
XM_017009969.2:c.14301A>G	XP_016865458.1:p.Pro4767=
XM_017009970.2:c.14301A>G	XP_016865459.1:p.Pro4767=
XM_017009971.2:c.14301A>G	XP_016865460.1:p.Pro4767=
XM_017009972.1:c.7419A>G	XP_016865461.1:p.Pro2473=
XM_017009973.1:c.7398A>G	XP_016865462.1:p.Pro2466=
NR_003149.2:n.14296A>G