Canonical Allele Identifier: CA2578359522

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90708863del , CM000667.2:g.90708863del	GRCh38
NC_000005.9:g.90004680del , CM000667.1:g.90004680del	GRCh37
NC_000005.8:g.90040436del	NCBI36
NG_007083.1:g.155064del
NG_007083.2:g.184520del

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8778del MANE Select	NP_115495.3:p.Tyr2926Ter
ENST00000405460.9:c.8778del MANE Select	ENSP00000384582.2:p.Tyr2926Ter
NM_032119.3:c.8778del	NP_115495.3:p.Tyr2926Ter
NR_003149.1:n.8791del
NR_003149.2:n.8794del
ENST00000405460.6:c.8778del	ENSP00000384582.2:p.Tyr2926Ter
ENST00000509621.1:c.1475del
ENST00000639431.1:c.265+32654del	ENSP00000491057.1:n.265+32654del
ENST00000639473.1:n.4237del
ENST00000640012.1:c.2585del
ENST00000640374.1:n.1922del
ENST00000640403.1:c.6069del	ENSP00000492531.1:p.Tyr2023Ter
ENST00000640779.1:c.3507del
XM_011543675.1:c.8775del	XP_011541977.1:p.Tyr2925Ter
XM_011543676.1:c.8697del	XP_011541978.1:p.Tyr2899Ter
XM_011543677.1:c.6081del	XP_011541979.1:p.Tyr2027Ter
XM_011543678.1:c.8778del	XP_011541980.1:p.Tyr2926Ter
XM_011543679.1:c.8778del	XP_011541981.1:p.Tyr2926Ter
XM_017009963.2:c.8799del	XP_016865452.1:p.Tyr2933Ter
XM_017009964.2:c.8796del	XP_016865453.1:p.Tyr2932Ter
XM_017009965.1:c.8796del	XP_016865454.1:p.Tyr2932Ter
XM_017009966.2:c.8718del	XP_016865455.1:p.Tyr2906Ter
XM_017009967.1:c.8703del	XP_016865456.1:p.Tyr2901Ter
XM_017009968.2:c.8799del	XP_016865457.1:p.Tyr2933Ter
XM_017009969.2:c.8799del	XP_016865458.1:p.Tyr2933Ter
XM_017009970.2:c.8799del	XP_016865459.1:p.Tyr2933Ter
XM_017009971.2:c.8799del	XP_016865460.1:p.Tyr2933Ter
XM_017009972.1:c.1917del	XP_016865461.1:p.Tyr639Ter
XM_017009973.1:c.1896del	XP_016865462.1:p.Tyr632Ter
XM_017009974.2:c.8799del	XP_016865463.1:p.Tyr2933Ter