Canonical Allele Identifier: CA1562869773

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720077G= , CM000667.2:g.90720077G=	GRCh38
NC_000005.9:g.90015894G= , CM000667.1:g.90015894G=	GRCh37
NC_000005.8:g.90051650G=	NCBI36
NG_007083.1:g.166278G=
NG_007083.2:g.195734G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9477G= MANE Select	NP_115495.3:p.Thr3159=
ENST00000405460.9:c.9477G= MANE Select	ENSP00000384582.2:p.Thr3159=
NM_032119.3:c.9477G=	NP_115495.3:p.Thr3159=
NR_003149.1:n.9490G=
NR_003149.2:n.9493G=
ENST00000405460.6:c.9477G=	ENSP00000384582.2:p.Thr3159=
ENST00000509621.1:c.2174G=
ENST00000639431.1:c.265+43868G=	ENSP00000491057.1:n.265+43868G=
ENST00000640374.1:n.2621G=
ENST00000640779.1:c.4206G=
XM_011543675.1:c.9474G=	XP_011541977.1:p.Thr3158=
XM_011543676.1:c.9396G=	XP_011541978.1:p.Thr3132=
XM_011543677.1:c.6780G=	XP_011541979.1:p.Thr2260=
XM_011543678.1:c.9477G=	XP_011541980.1:p.Thr3159=
XM_011543679.1:c.9477G=	XP_011541981.1:p.Thr3159=
XM_017009963.2:c.9498G=	XP_016865452.1:p.Thr3166=
XM_017009964.2:c.9495G=	XP_016865453.1:p.Thr3165=
XM_017009965.1:c.9495G=	XP_016865454.1:p.Thr3165=
XM_017009966.2:c.9417G=	XP_016865455.1:p.Thr3139=
XM_017009967.1:c.9402G=	XP_016865456.1:p.Thr3134=
XM_017009968.2:c.9498G=	XP_016865457.1:p.Thr3166=
XM_017009969.2:c.9498G=	XP_016865458.1:p.Thr3166=
XM_017009970.2:c.9498G=	XP_016865459.1:p.Thr3166=
XM_017009971.2:c.9498G=	XP_016865460.1:p.Thr3166=
XM_017009972.1:c.2616G=	XP_016865461.1:p.Thr872=
XM_017009973.1:c.2595G=	XP_016865462.1:p.Thr865=
XM_017009974.2:c.9498G=	XP_016865463.1:p.Thr3166=
XR_001742802.1:n.2523-4268C=
XR_948560.1:n.272-4268C=