Canonical Allele Identifier: CA1562882064

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745607T= , CM000667.2:g.90745607T=	GRCh38
NC_000005.9:g.90041424T= , CM000667.1:g.90041424T=	GRCh37
NC_000005.8:g.90077180T=	NCBI36
NG_007083.1:g.191808T=
NG_007083.2:g.221264T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10786T= MANE Select	ENSP00000384582.2:p.Phe3596=
ENST00000639431.1:c.265+69398T=	ENSP00000491057.1:n.265+69398T=
ENST00000640374.1:n.3930T=
ENST00000640464.1:n.1205T=
ENST00000405460.6:c.10786T=	ENSP00000384582.2:p.Phe3596=
ENST00000509621.1:c.3483T=
NM_032119.3:c.10786T=	NP_115495.3:p.Phe3596=
NR_003149.1:n.10799T=
XM_011543675.1:c.10783T=	XP_011541977.1:p.Phe3595=
XM_011543676.1:c.10705T=	XP_011541978.1:p.Phe3569=
XM_011543677.1:c.8089T=	XP_011541979.1:p.Phe2697=
XM_011543678.1:c.10786T=	XP_011541980.1:p.Phe3596=
XM_011543679.1:c.*8T=	XP_011541981.1:n.*8T=
NM_032119.4:c.10786T= MANE Select	NP_115495.3:p.Phe3596=
XM_017009963.2:c.10807T=	XP_016865452.1:p.Phe3603=
XM_017009964.2:c.10804T=	XP_016865453.1:p.Phe3602=
XM_017009965.1:c.10804T=	XP_016865454.1:p.Phe3602=
XM_017009966.2:c.10726T=	XP_016865455.1:p.Phe3576=
XM_017009967.1:c.10711T=	XP_016865456.1:p.Phe3571=
XM_017009968.2:c.10807T=	XP_016865457.1:p.Phe3603=
XM_017009969.2:c.10807T=	XP_016865458.1:p.Phe3603=
XM_017009970.2:c.10807T=	XP_016865459.1:p.Phe3603=
XM_017009971.2:c.10807T=	XP_016865460.1:p.Phe3603=
XM_017009972.1:c.3925T=	XP_016865461.1:p.Phe1309=
XM_017009973.1:c.3904T=	XP_016865462.1:p.Phe1302=
XM_017009974.2:c.*8T=	XP_016865463.1:n.*8T=
NR_003149.2:n.10802T=