Canonical Allele Identifier: CA360397658

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012495T>G (hg19) ; chr5:g.90716678T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716678T>G , CM000667.2:g.90716678T>G	GRCh38
NC_000005.9:g.90012495T>G , CM000667.1:g.90012495T>G	GRCh37
NC_000005.8:g.90048251T>G	NCBI36
NG_007083.1:g.162879T>G
NG_007083.2:g.192335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9396T>G MANE Select	ENSP00000384582.2:p.Asp3132Glu
ENST00000639431.1:c.265+40469T>G	ENSP00000491057.1:n.265+40469T>G
ENST00000639473.1:n.4855T>G
ENST00000640012.1:c.3203T>G
ENST00000640374.1:n.2540T>G
ENST00000640779.1:c.4125T>G
ENST00000405460.6:c.9396T>G	ENSP00000384582.2:p.Asp3132Glu
ENST00000509621.1:c.2093T>G
NM_032119.3:c.9396T>G	NP_115495.3:p.Asp3132Glu
NR_003149.1:n.9409T>G
XM_011543675.1:c.9393T>G	XP_011541977.1:p.Asp3131Glu
XM_011543676.1:c.9315T>G	XP_011541978.1:p.Asp3105Glu
XM_011543677.1:c.6699T>G	XP_011541979.1:p.Asp2233Glu
XM_011543678.1:c.9396T>G	XP_011541980.1:p.Asp3132Glu
XM_011543679.1:c.9396T>G	XP_011541981.1:p.Asp3132Glu
XR_948560.1:n.272-869A>C
NM_032119.4:c.9396T>G MANE Select	NP_115495.3:p.Asp3132Glu
XM_017009963.2:c.9417T>G	XP_016865452.1:p.Asp3139Glu
XM_017009964.2:c.9414T>G	XP_016865453.1:p.Asp3138Glu
XM_017009965.1:c.9414T>G	XP_016865454.1:p.Asp3138Glu
XM_017009966.2:c.9336T>G	XP_016865455.1:p.Asp3112Glu
XM_017009967.1:c.9321T>G	XP_016865456.1:p.Asp3107Glu
XM_017009968.2:c.9417T>G	XP_016865457.1:p.Asp3139Glu
XM_017009969.2:c.9417T>G	XP_016865458.1:p.Asp3139Glu
XM_017009970.2:c.9417T>G	XP_016865459.1:p.Asp3139Glu
XM_017009971.2:c.9417T>G	XP_016865460.1:p.Asp3139Glu
XM_017009972.1:c.2535T>G	XP_016865461.1:p.Asp845Glu
XM_017009973.1:c.2514T>G	XP_016865462.1:p.Asp838Glu
XM_017009974.2:c.9417T>G	XP_016865463.1:p.Asp3139Glu
XR_001742802.1:n.2523-869A>C
NR_003149.2:n.9412T>G