Canonical Allele Identifier: CA1562836902

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644778T= , CM000667.2:g.90644778T=	GRCh38
NC_000005.9:g.89940595T= , CM000667.1:g.89940595T=	GRCh37
NC_000005.8:g.89976351T=	NCBI36
NG_007083.1:g.90979T=
NG_007083.2:g.120435T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2807T= MANE Select	ENSP00000384582.2:p.Phe936=
ENST00000504142.2:n.1573T=
ENST00000639676.1:n.405T=
ENST00000640403.1:c.110T=	ENSP00000492531.1:p.Phe37=
ENST00000405460.6:c.2807T=	ENSP00000384582.2:p.Phe936=
ENST00000504142.1:c.1572T=
NM_032119.3:c.2807T=	NP_115495.3:p.Phe936=
NR_003149.1:n.2903T=
XM_011543675.1:c.2807T=	XP_011541977.1:p.Phe936=
XM_011543676.1:c.2807T=	XP_011541978.1:p.Phe936=
XM_011543677.1:c.110T=	XP_011541979.1:p.Phe37=
XM_011543678.1:c.2807T=	XP_011541980.1:p.Phe936=
XM_011543679.1:c.2807T=	XP_011541981.1:p.Phe936=
NM_032119.4:c.2807T= MANE Select	NP_115495.3:p.Phe936=
XM_017009963.2:c.2807T=	XP_016865452.1:p.Phe936=
XM_017009964.2:c.2807T=	XP_016865453.1:p.Phe936=
XM_017009965.1:c.2804T=	XP_016865454.1:p.Phe935=
XM_017009966.2:c.2807T=	XP_016865455.1:p.Phe936=
XM_017009967.1:c.2711T=	XP_016865456.1:p.Phe904=
XM_017009968.2:c.2807T=	XP_016865457.1:p.Phe936=
XM_017009969.2:c.2807T=	XP_016865458.1:p.Phe936=
XM_017009970.2:c.2807T=	XP_016865459.1:p.Phe936=
XM_017009971.2:c.2807T=	XP_016865460.1:p.Phe936=
XM_017009974.2:c.2807T=	XP_016865463.1:p.Phe936=
NR_003149.2:n.2906T=