Canonical Allele Identifier: CA1562867521

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712298T= , CM000667.2:g.90712298T=	GRCh38
NC_000005.9:g.90008115T= , CM000667.1:g.90008115T=	GRCh37
NC_000005.8:g.90043871T=	NCBI36
NG_007083.1:g.158499T=
NG_007083.2:g.187955T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9054T= MANE Select	ENSP00000384582.2:p.Phe3018=
ENST00000639431.1:c.265+36089T=	ENSP00000491057.1:n.265+36089T=
ENST00000639473.1:n.4513T=
ENST00000640012.1:c.2861T=
ENST00000640374.1:n.2198T=
ENST00000640779.1:c.3783T=
ENST00000405460.6:c.9054T=	ENSP00000384582.2:p.Phe3018=
ENST00000509621.1:c.1751T=
NM_032119.3:c.9054T=	NP_115495.3:p.Phe3018=
NR_003149.1:n.9067T=
XM_011543675.1:c.9051T=	XP_011541977.1:p.Phe3017=
XM_011543676.1:c.8973T=	XP_011541978.1:p.Phe2991=
XM_011543677.1:c.6357T=	XP_011541979.1:p.Phe2119=
XM_011543678.1:c.9054T=	XP_011541980.1:p.Phe3018=
XM_011543679.1:c.9054T=	XP_011541981.1:p.Phe3018=
NM_032119.4:c.9054T= MANE Select	NP_115495.3:p.Phe3018=
XM_017009963.2:c.9075T=	XP_016865452.1:p.Phe3025=
XM_017009964.2:c.9072T=	XP_016865453.1:p.Phe3024=
XM_017009965.1:c.9072T=	XP_016865454.1:p.Phe3024=
XM_017009966.2:c.8994T=	XP_016865455.1:p.Phe2998=
XM_017009967.1:c.8979T=	XP_016865456.1:p.Phe2993=
XM_017009968.2:c.9075T=	XP_016865457.1:p.Phe3025=
XM_017009969.2:c.9075T=	XP_016865458.1:p.Phe3025=
XM_017009970.2:c.9075T=	XP_016865459.1:p.Phe3025=
XM_017009971.2:c.9075T=	XP_016865460.1:p.Phe3025=
XM_017009972.1:c.2193T=	XP_016865461.1:p.Phe731=
XM_017009973.1:c.2172T=	XP_016865462.1:p.Phe724=
XM_017009974.2:c.9075T=	XP_016865463.1:p.Phe3025=
NR_003149.2:n.9070T=