Canonical Allele Identifier: CA1562867528

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712315A= , CM000667.2:g.90712315A=	GRCh38
NC_000005.9:g.90008132A= , CM000667.1:g.90008132A=	GRCh37
NC_000005.8:g.90043888A=	NCBI36
NG_007083.1:g.158516A=
NG_007083.2:g.187972A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9071A= MANE Select	ENSP00000384582.2:p.Tyr3024=
ENST00000639431.1:c.265+36106A=	ENSP00000491057.1:n.265+36106A=
ENST00000639473.1:n.4530A=
ENST00000640012.1:c.2878A=
ENST00000640374.1:n.2215A=
ENST00000640779.1:c.3800A=
ENST00000405460.6:c.9071A=	ENSP00000384582.2:p.Tyr3024=
ENST00000509621.1:c.1768A=
NM_032119.3:c.9071A=	NP_115495.3:p.Tyr3024=
NR_003149.1:n.9084A=
XM_011543675.1:c.9068A=	XP_011541977.1:p.Tyr3023=
XM_011543676.1:c.8990A=	XP_011541978.1:p.Tyr2997=
XM_011543677.1:c.6374A=	XP_011541979.1:p.Tyr2125=
XM_011543678.1:c.9071A=	XP_011541980.1:p.Tyr3024=
XM_011543679.1:c.9071A=	XP_011541981.1:p.Tyr3024=
NM_032119.4:c.9071A= MANE Select	NP_115495.3:p.Tyr3024=
XM_017009963.2:c.9092A=	XP_016865452.1:p.Tyr3031=
XM_017009964.2:c.9089A=	XP_016865453.1:p.Tyr3030=
XM_017009965.1:c.9089A=	XP_016865454.1:p.Tyr3030=
XM_017009966.2:c.9011A=	XP_016865455.1:p.Tyr3004=
XM_017009967.1:c.8996A=	XP_016865456.1:p.Tyr2999=
XM_017009968.2:c.9092A=	XP_016865457.1:p.Tyr3031=
XM_017009969.2:c.9092A=	XP_016865458.1:p.Tyr3031=
XM_017009970.2:c.9092A=	XP_016865459.1:p.Tyr3031=
XM_017009971.2:c.9092A=	XP_016865460.1:p.Tyr3031=
XM_017009972.1:c.2210A=	XP_016865461.1:p.Tyr737=
XM_017009973.1:c.2189A=	XP_016865462.1:p.Tyr730=
XM_017009974.2:c.9092A=	XP_016865463.1:p.Tyr3031=
NR_003149.2:n.9087A=