Canonical Allele Identifier: CA360397647

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012493G>A (hg19) ; chr5:g.90716676G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716676G>A , CM000667.2:g.90716676G>A	GRCh38
NC_000005.9:g.90012493G>A , CM000667.1:g.90012493G>A	GRCh37
NC_000005.8:g.90048249G>A	NCBI36
NG_007083.1:g.162877G>A
NG_007083.2:g.192333G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9394G>A MANE Select	ENSP00000384582.2:p.Asp3132Asn
ENST00000639431.1:c.265+40467G>A	ENSP00000491057.1:n.265+40467G>A
ENST00000639473.1:n.4853G>A
ENST00000640012.1:c.3201G>A
ENST00000640374.1:n.2538G>A
ENST00000640779.1:c.4123G>A
ENST00000405460.6:c.9394G>A	ENSP00000384582.2:p.Asp3132Asn
ENST00000509621.1:c.2091G>A
NM_032119.3:c.9394G>A	NP_115495.3:p.Asp3132Asn
NR_003149.1:n.9407G>A
XM_011543675.1:c.9391G>A	XP_011541977.1:p.Asp3131Asn
XM_011543676.1:c.9313G>A	XP_011541978.1:p.Asp3105Asn
XM_011543677.1:c.6697G>A	XP_011541979.1:p.Asp2233Asn
XM_011543678.1:c.9394G>A	XP_011541980.1:p.Asp3132Asn
XM_011543679.1:c.9394G>A	XP_011541981.1:p.Asp3132Asn
XR_948560.1:n.272-867C>T
NM_032119.4:c.9394G>A MANE Select	NP_115495.3:p.Asp3132Asn
XM_017009963.2:c.9415G>A	XP_016865452.1:p.Asp3139Asn
XM_017009964.2:c.9412G>A	XP_016865453.1:p.Asp3138Asn
XM_017009965.1:c.9412G>A	XP_016865454.1:p.Asp3138Asn
XM_017009966.2:c.9334G>A	XP_016865455.1:p.Asp3112Asn
XM_017009967.1:c.9319G>A	XP_016865456.1:p.Asp3107Asn
XM_017009968.2:c.9415G>A	XP_016865457.1:p.Asp3139Asn
XM_017009969.2:c.9415G>A	XP_016865458.1:p.Asp3139Asn
XM_017009970.2:c.9415G>A	XP_016865459.1:p.Asp3139Asn
XM_017009971.2:c.9415G>A	XP_016865460.1:p.Asp3139Asn
XM_017009972.1:c.2533G>A	XP_016865461.1:p.Asp845Asn
XM_017009973.1:c.2512G>A	XP_016865462.1:p.Asp838Asn
XM_017009974.2:c.9415G>A	XP_016865463.1:p.Asp3139Asn
XR_001742802.1:n.2523-867C>T
NR_003149.2:n.9410G>A