Canonical Allele Identifier: CA360401213

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90086915A>G (hg19) ; chr5:g.90791098A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90791098A>G , CM000667.2:g.90791098A>G	GRCh38
NC_000005.9:g.90086915A>G , CM000667.1:g.90086915A>G	GRCh37
NC_000005.8:g.90122671A>G	NCBI36
NG_007083.1:g.237299A>G
NG_007083.2:g.266755A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.14269A>G MANE Select	ENSP00000384582.2:p.Asn4757Asp
ENST00000425867.3:c.3223A>G	ENSP00000392618.3:p.Asn1075Asp
ENST00000638510.1:n.1536A>G
ENST00000638585.1:n.35A>G
ENST00000638975.1:c.898A>G	ENSP00000492630.1:p.Asn300Asp
ENST00000639431.1:c.265+114889A>G	ENSP00000491057.1:n.265+114889A>G
ENST00000640407.1:c.679A>G	ENSP00000491425.1:p.Asn227Asp
ENST00000405460.6:c.14269A>G	ENSP00000384582.2:p.Asn4757Asp
ENST00000425867.2:c.1252A>G	ENSP00000392618.2:p.Asn418Asp
NM_032119.3:c.14269A>G	NP_115495.3:p.Asn4757Asp
NR_003149.1:n.14282A>G
XM_011543675.1:c.14266A>G	XP_011541977.1:p.Asn4756Asp
XM_011543676.1:c.14188A>G	XP_011541978.1:p.Asn4730Asp
XM_011543677.1:c.11572A>G	XP_011541979.1:p.Asn3858Asp
XM_011543678.1:c.14269A>G	XP_011541980.1:p.Asn4757Asp
NM_032119.4:c.14269A>G MANE Select	NP_115495.3:p.Asn4757Asp
XM_017009963.2:c.14290A>G	XP_016865452.1:p.Asn4764Asp
XM_017009964.2:c.14287A>G	XP_016865453.1:p.Asn4763Asp
XM_017009965.1:c.14287A>G	XP_016865454.1:p.Asn4763Asp
XM_017009966.2:c.14209A>G	XP_016865455.1:p.Asn4737Asp
XM_017009967.1:c.14194A>G	XP_016865456.1:p.Asn4732Asp
XM_017009968.2:c.14290A>G	XP_016865457.1:p.Asn4764Asp
XM_017009969.2:c.14290A>G	XP_016865458.1:p.Asn4764Asp
XM_017009970.2:c.14290A>G	XP_016865459.1:p.Asn4764Asp
XM_017009971.2:c.14290A>G	XP_016865460.1:p.Asn4764Asp
XM_017009972.1:c.7408A>G	XP_016865461.1:p.Asn2470Asp
XM_017009973.1:c.7387A>G	XP_016865462.1:p.Asn2463Asp
NR_003149.2:n.14285A>G