Canonical Allele Identifier: CA1562870624

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716669A= , CM000667.2:g.90716669A=	GRCh38
NC_000005.9:g.90012486A= , CM000667.1:g.90012486A=	GRCh37
NC_000005.8:g.90048242A=	NCBI36
NG_007083.1:g.162870A=
NG_007083.2:g.192326A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9387A= MANE Select	ENSP00000384582.2:p.Glu3129=
ENST00000639431.1:c.265+40460A=	ENSP00000491057.1:n.265+40460A=
ENST00000639473.1:n.4846A=
ENST00000640012.1:c.3194A=
ENST00000640374.1:n.2531A=
ENST00000640779.1:c.4116A=
ENST00000405460.6:c.9387A=	ENSP00000384582.2:p.Glu3129=
ENST00000509621.1:c.2084A=
NM_032119.3:c.9387A=	NP_115495.3:p.Glu3129=
NR_003149.1:n.9400A=
XM_011543675.1:c.9384A=	XP_011541977.1:p.Glu3128=
XM_011543676.1:c.9306A=	XP_011541978.1:p.Glu3102=
XM_011543677.1:c.6690A=	XP_011541979.1:p.Glu2230=
XM_011543678.1:c.9387A=	XP_011541980.1:p.Glu3129=
XM_011543679.1:c.9387A=	XP_011541981.1:p.Glu3129=
XR_948560.1:n.272-860T=
NM_032119.4:c.9387A= MANE Select	NP_115495.3:p.Glu3129=
XM_017009963.2:c.9408A=	XP_016865452.1:p.Glu3136=
XM_017009964.2:c.9405A=	XP_016865453.1:p.Glu3135=
XM_017009965.1:c.9405A=	XP_016865454.1:p.Glu3135=
XM_017009966.2:c.9327A=	XP_016865455.1:p.Glu3109=
XM_017009967.1:c.9312A=	XP_016865456.1:p.Glu3104=
XM_017009968.2:c.9408A=	XP_016865457.1:p.Glu3136=
XM_017009969.2:c.9408A=	XP_016865458.1:p.Glu3136=
XM_017009970.2:c.9408A=	XP_016865459.1:p.Glu3136=
XM_017009971.2:c.9408A=	XP_016865460.1:p.Glu3136=
XM_017009972.1:c.2526A=	XP_016865461.1:p.Glu842=
XM_017009973.1:c.2505A=	XP_016865462.1:p.Glu835=
XM_017009974.2:c.9408A=	XP_016865463.1:p.Glu3136=
XR_001742802.1:n.2523-860T=
NR_003149.2:n.9403A=