Canonical Allele Identifier: CA1562859312

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692738A= , CM000667.2:g.90692738A=	GRCh38
NC_000005.9:g.89988555A= , CM000667.1:g.89988555A=	GRCh37
NC_000005.8:g.90024311A=	NCBI36
NG_007083.1:g.138939A=
NG_007083.2:g.168395A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7085A= MANE Select	ENSP00000384582.2:p.Gln2362=
ENST00000639431.1:c.265+16529A=	ENSP00000491057.1:n.265+16529A=
ENST00000639473.1:n.2544A=
ENST00000640012.1:c.892A=
ENST00000640374.1:n.229A=
ENST00000640403.1:c.4376A=	ENSP00000492531.1:p.Gln1459=
ENST00000640779.1:c.1814A=
ENST00000405460.6:c.7085A=	ENSP00000384582.2:p.Gln2362=
NM_032119.3:c.7085A=	NP_115495.3:p.Gln2362=
NR_003149.1:n.7098A=
XM_011543675.1:c.7082A=	XP_011541977.1:p.Gln2361=
XM_011543676.1:c.7004A=	XP_011541978.1:p.Gln2335=
XM_011543677.1:c.4388A=	XP_011541979.1:p.Gln1463=
XM_011543678.1:c.7085A=	XP_011541980.1:p.Gln2362=
XM_011543679.1:c.7085A=	XP_011541981.1:p.Gln2362=
NM_032119.4:c.7085A= MANE Select	NP_115495.3:p.Gln2362=
XM_017009963.2:c.7085A=	XP_016865452.1:p.Gln2362=
XM_017009964.2:c.7082A=	XP_016865453.1:p.Gln2361=
XM_017009965.1:c.7082A=	XP_016865454.1:p.Gln2361=
XM_017009966.2:c.7004A=	XP_016865455.1:p.Gln2335=
XM_017009967.1:c.6989A=	XP_016865456.1:p.Gln2330=
XM_017009968.2:c.7085A=	XP_016865457.1:p.Gln2362=
XM_017009969.2:c.7085A=	XP_016865458.1:p.Gln2362=
XM_017009970.2:c.7085A=	XP_016865459.1:p.Gln2362=
XM_017009971.2:c.7085A=	XP_016865460.1:p.Gln2362=
XM_017009972.1:c.203A=	XP_016865461.1:p.Gln68=
XM_017009973.1:c.203A=	XP_016865462.1:p.Gln68=
XM_017009974.2:c.7085A=	XP_016865463.1:p.Gln2362=
NR_003149.2:n.7101A=