Canonical Allele Identifier: CA1562867538

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712346T= , CM000667.2:g.90712346T=	GRCh38
NC_000005.9:g.90008163T= , CM000667.1:g.90008163T=	GRCh37
NC_000005.8:g.90043919T=	NCBI36
NG_007083.1:g.158547T=
NG_007083.2:g.188003T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9102T= MANE Select	ENSP00000384582.2:p.Asp3034=
ENST00000639431.1:c.265+36137T=	ENSP00000491057.1:n.265+36137T=
ENST00000639473.1:n.4561T=
ENST00000640012.1:c.2909T=
ENST00000640374.1:n.2246T=
ENST00000640779.1:c.3831T=
ENST00000405460.6:c.9102T=	ENSP00000384582.2:p.Asp3034=
ENST00000509621.1:c.1799T=
NM_032119.3:c.9102T=	NP_115495.3:p.Asp3034=
NR_003149.1:n.9115T=
XM_011543675.1:c.9099T=	XP_011541977.1:p.Asp3033=
XM_011543676.1:c.9021T=	XP_011541978.1:p.Asp3007=
XM_011543677.1:c.6405T=	XP_011541979.1:p.Asp2135=
XM_011543678.1:c.9102T=	XP_011541980.1:p.Asp3034=
XM_011543679.1:c.9102T=	XP_011541981.1:p.Asp3034=
NM_032119.4:c.9102T= MANE Select	NP_115495.3:p.Asp3034=
XM_017009963.2:c.9123T=	XP_016865452.1:p.Asp3041=
XM_017009964.2:c.9120T=	XP_016865453.1:p.Asp3040=
XM_017009965.1:c.9120T=	XP_016865454.1:p.Asp3040=
XM_017009966.2:c.9042T=	XP_016865455.1:p.Asp3014=
XM_017009967.1:c.9027T=	XP_016865456.1:p.Asp3009=
XM_017009968.2:c.9123T=	XP_016865457.1:p.Asp3041=
XM_017009969.2:c.9123T=	XP_016865458.1:p.Asp3041=
XM_017009970.2:c.9123T=	XP_016865459.1:p.Asp3041=
XM_017009971.2:c.9123T=	XP_016865460.1:p.Asp3041=
XM_017009972.1:c.2241T=	XP_016865461.1:p.Asp747=
XM_017009973.1:c.2220T=	XP_016865462.1:p.Asp740=
XM_017009974.2:c.9123T=	XP_016865463.1:p.Asp3041=
NR_003149.2:n.9118T=