Canonical Allele Identifier: CA1562867543

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712364T= , CM000667.2:g.90712364T=	GRCh38
NC_000005.9:g.90008181T= , CM000667.1:g.90008181T=	GRCh37
NC_000005.8:g.90043937T=	NCBI36
NG_007083.1:g.158565T=
NG_007083.2:g.188021T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9120T= MANE Select	ENSP00000384582.2:p.Asp3040=
ENST00000639431.1:c.265+36155T=	ENSP00000491057.1:n.265+36155T=
ENST00000639473.1:n.4579T=
ENST00000640012.1:c.2927T=
ENST00000640374.1:n.2264T=
ENST00000640779.1:c.3849T=
ENST00000405460.6:c.9120T=	ENSP00000384582.2:p.Asp3040=
ENST00000509621.1:c.1817T=
NM_032119.3:c.9120T=	NP_115495.3:p.Asp3040=
NR_003149.1:n.9133T=
XM_011543675.1:c.9117T=	XP_011541977.1:p.Asp3039=
XM_011543676.1:c.9039T=	XP_011541978.1:p.Asp3013=
XM_011543677.1:c.6423T=	XP_011541979.1:p.Asp2141=
XM_011543678.1:c.9120T=	XP_011541980.1:p.Asp3040=
XM_011543679.1:c.9120T=	XP_011541981.1:p.Asp3040=
NM_032119.4:c.9120T= MANE Select	NP_115495.3:p.Asp3040=
XM_017009963.2:c.9141T=	XP_016865452.1:p.Asp3047=
XM_017009964.2:c.9138T=	XP_016865453.1:p.Asp3046=
XM_017009965.1:c.9138T=	XP_016865454.1:p.Asp3046=
XM_017009966.2:c.9060T=	XP_016865455.1:p.Asp3020=
XM_017009967.1:c.9045T=	XP_016865456.1:p.Asp3015=
XM_017009968.2:c.9141T=	XP_016865457.1:p.Asp3047=
XM_017009969.2:c.9141T=	XP_016865458.1:p.Asp3047=
XM_017009970.2:c.9141T=	XP_016865459.1:p.Asp3047=
XM_017009971.2:c.9141T=	XP_016865460.1:p.Asp3047=
XM_017009972.1:c.2259T=	XP_016865461.1:p.Asp753=
XM_017009973.1:c.2238T=	XP_016865462.1:p.Asp746=
XM_017009974.2:c.9141T=	XP_016865463.1:p.Asp3047=
NR_003149.2:n.9136T=