Canonical Allele Identifier: CA360409572

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041577A>G (hg19) ; chr5:g.90745760A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745760A>G , CM000667.2:g.90745760A>G	GRCh38
NC_000005.9:g.90041577A>G , CM000667.1:g.90041577A>G	GRCh37
NC_000005.8:g.90077333A>G	NCBI36
NG_007083.1:g.191961A>G
NG_007083.2:g.221417A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10939A>G MANE Select	ENSP00000384582.2:p.Asn3647Asp
ENST00000425867.3:c.70A>G	ENSP00000392618.3:p.Asn24Asp
ENST00000639431.1:c.265+69551A>G	ENSP00000491057.1:n.265+69551A>G
ENST00000640374.1:n.4083A>G
ENST00000640464.1:n.1358A>G
ENST00000405460.6:c.10939A>G	ENSP00000384582.2:p.Asn3647Asp
ENST00000509621.1:c.3636A>G
NM_032119.3:c.10939A>G	NP_115495.3:p.Asn3647Asp
NR_003149.1:n.10952A>G
XM_011543675.1:c.10936A>G	XP_011541977.1:p.Asn3646Asp
XM_011543676.1:c.10858A>G	XP_011541978.1:p.Asn3620Asp
XM_011543677.1:c.8242A>G	XP_011541979.1:p.Asn2748Asp
XM_011543678.1:c.10939A>G	XP_011541980.1:p.Asn3647Asp
NM_032119.4:c.10939A>G MANE Select	NP_115495.3:p.Asn3647Asp
XM_017009963.2:c.10960A>G	XP_016865452.1:p.Asn3654Asp
XM_017009964.2:c.10957A>G	XP_016865453.1:p.Asn3653Asp
XM_017009965.1:c.10957A>G	XP_016865454.1:p.Asn3653Asp
XM_017009966.2:c.10879A>G	XP_016865455.1:p.Asn3627Asp
XM_017009967.1:c.10864A>G	XP_016865456.1:p.Asn3622Asp
XM_017009968.2:c.10960A>G	XP_016865457.1:p.Asn3654Asp
XM_017009969.2:c.10960A>G	XP_016865458.1:p.Asn3654Asp
XM_017009970.2:c.10960A>G	XP_016865459.1:p.Asn3654Asp
XM_017009971.2:c.10960A>G	XP_016865460.1:p.Asn3654Asp
XM_017009972.1:c.4078A>G	XP_016865461.1:p.Asn1360Asp
XM_017009973.1:c.4057A>G	XP_016865462.1:p.Asn1353Asp
NR_003149.2:n.10955A>G