Canonical Allele Identifier: CA360397019

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716490G>T , CM000667.2:g.90716490G>T	GRCh38
NC_000005.9:g.90012307G>T , CM000667.1:g.90012307G>T	GRCh37
NC_000005.8:g.90048063G>T	NCBI36
NG_007083.1:g.162691G>T
NG_007083.2:g.192147G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9208G>T MANE Select	NP_115495.3:p.Asp3070Tyr
ENST00000405460.9:c.9208G>T MANE Select	ENSP00000384582.2:p.Asp3070Tyr
NM_032119.3:c.9208G>T	NP_115495.3:p.Asp3070Tyr
NR_003149.1:n.9221G>T
NR_003149.2:n.9224G>T
ENST00000405460.6:c.9208G>T	ENSP00000384582.2:p.Asp3070Tyr
ENST00000509621.1:c.1905G>T
ENST00000639431.1:c.265+40281G>T	ENSP00000491057.1:n.265+40281G>T
ENST00000639473.1:n.4667G>T
ENST00000640012.1:c.3015G>T
ENST00000640374.1:n.2352G>T
ENST00000640779.1:c.3937G>T
XM_011543675.1:c.9205G>T	XP_011541977.1:p.Asp3069Tyr
XM_011543676.1:c.9127G>T	XP_011541978.1:p.Asp3043Tyr
XM_011543677.1:c.6511G>T	XP_011541979.1:p.Asp2171Tyr
XM_011543678.1:c.9208G>T	XP_011541980.1:p.Asp3070Tyr
XM_011543679.1:c.9208G>T	XP_011541981.1:p.Asp3070Tyr
XM_017009963.2:c.9229G>T	XP_016865452.1:p.Asp3077Tyr
XM_017009964.2:c.9226G>T	XP_016865453.1:p.Asp3076Tyr
XM_017009965.1:c.9226G>T	XP_016865454.1:p.Asp3076Tyr
XM_017009966.2:c.9148G>T	XP_016865455.1:p.Asp3050Tyr
XM_017009967.1:c.9133G>T	XP_016865456.1:p.Asp3045Tyr
XM_017009968.2:c.9229G>T	XP_016865457.1:p.Asp3077Tyr
XM_017009969.2:c.9229G>T	XP_016865458.1:p.Asp3077Tyr
XM_017009970.2:c.9229G>T	XP_016865459.1:p.Asp3077Tyr
XM_017009971.2:c.9229G>T	XP_016865460.1:p.Asp3077Tyr
XM_017009972.1:c.2347G>T	XP_016865461.1:p.Asp783Tyr
XM_017009973.1:c.2326G>T	XP_016865462.1:p.Asp776Tyr
XM_017009974.2:c.9229G>T	XP_016865463.1:p.Asp3077Tyr
XR_001742802.1:n.2523-681C>A
XR_948560.1:n.272-681C>A