Canonical Allele Identifier: CA360399386

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720072G>T , CM000667.2:g.90720072G>T	GRCh38
NC_000005.9:g.90015889G>T , CM000667.1:g.90015889G>T	GRCh37
NC_000005.8:g.90051645G>T	NCBI36
NG_007083.1:g.166273G>T
NG_007083.2:g.195729G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9472G>T MANE Select	NP_115495.3:p.Asp3158Tyr
ENST00000405460.9:c.9472G>T MANE Select	ENSP00000384582.2:p.Asp3158Tyr
NM_032119.3:c.9472G>T	NP_115495.3:p.Asp3158Tyr
NR_003149.1:n.9485G>T
NR_003149.2:n.9488G>T
ENST00000405460.6:c.9472G>T	ENSP00000384582.2:p.Asp3158Tyr
ENST00000509621.1:c.2169G>T
ENST00000639431.1:c.265+43863G>T	ENSP00000491057.1:n.265+43863G>T
ENST00000640374.1:n.2616G>T
ENST00000640779.1:c.4201G>T
XM_011543675.1:c.9469G>T	XP_011541977.1:p.Asp3157Tyr
XM_011543676.1:c.9391G>T	XP_011541978.1:p.Asp3131Tyr
XM_011543677.1:c.6775G>T	XP_011541979.1:p.Asp2259Tyr
XM_011543678.1:c.9472G>T	XP_011541980.1:p.Asp3158Tyr
XM_011543679.1:c.9472G>T	XP_011541981.1:p.Asp3158Tyr
XM_017009963.2:c.9493G>T	XP_016865452.1:p.Asp3165Tyr
XM_017009964.2:c.9490G>T	XP_016865453.1:p.Asp3164Tyr
XM_017009965.1:c.9490G>T	XP_016865454.1:p.Asp3164Tyr
XM_017009966.2:c.9412G>T	XP_016865455.1:p.Asp3138Tyr
XM_017009967.1:c.9397G>T	XP_016865456.1:p.Asp3133Tyr
XM_017009968.2:c.9493G>T	XP_016865457.1:p.Asp3165Tyr
XM_017009969.2:c.9493G>T	XP_016865458.1:p.Asp3165Tyr
XM_017009970.2:c.9493G>T	XP_016865459.1:p.Asp3165Tyr
XM_017009971.2:c.9493G>T	XP_016865460.1:p.Asp3165Tyr
XM_017009972.1:c.2611G>T	XP_016865461.1:p.Asp871Tyr
XM_017009973.1:c.2590G>T	XP_016865462.1:p.Asp864Tyr
XM_017009974.2:c.9493G>T	XP_016865463.1:p.Asp3165Tyr
XR_001742802.1:n.2523-4263C>A
XR_948560.1:n.272-4263C>A