Canonical Allele Identifier: CA1562870618

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716643G= , CM000667.2:g.90716643G=	GRCh38
NC_000005.9:g.90012460G= , CM000667.1:g.90012460G=	GRCh37
NC_000005.8:g.90048216G=	NCBI36
NG_007083.1:g.162844G=
NG_007083.2:g.192300G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9361G= MANE Select	ENSP00000384582.2:p.Val3121=
ENST00000639431.1:c.265+40434G=	ENSP00000491057.1:n.265+40434G=
ENST00000639473.1:n.4820G=
ENST00000640012.1:c.3168G=
ENST00000640374.1:n.2505G=
ENST00000640779.1:c.4090G=
ENST00000405460.6:c.9361G=	ENSP00000384582.2:p.Val3121=
ENST00000509621.1:c.2058G=
NM_032119.3:c.9361G=	NP_115495.3:p.Val3121=
NR_003149.1:n.9374G=
XM_011543675.1:c.9358G=	XP_011541977.1:p.Val3120=
XM_011543676.1:c.9280G=	XP_011541978.1:p.Val3094=
XM_011543677.1:c.6664G=	XP_011541979.1:p.Val2222=
XM_011543678.1:c.9361G=	XP_011541980.1:p.Val3121=
XM_011543679.1:c.9361G=	XP_011541981.1:p.Val3121=
XR_948560.1:n.272-834C=
NM_032119.4:c.9361G= MANE Select	NP_115495.3:p.Val3121=
XM_017009963.2:c.9382G=	XP_016865452.1:p.Val3128=
XM_017009964.2:c.9379G=	XP_016865453.1:p.Val3127=
XM_017009965.1:c.9379G=	XP_016865454.1:p.Val3127=
XM_017009966.2:c.9301G=	XP_016865455.1:p.Val3101=
XM_017009967.1:c.9286G=	XP_016865456.1:p.Val3096=
XM_017009968.2:c.9382G=	XP_016865457.1:p.Val3128=
XM_017009969.2:c.9382G=	XP_016865458.1:p.Val3128=
XM_017009970.2:c.9382G=	XP_016865459.1:p.Val3128=
XM_017009971.2:c.9382G=	XP_016865460.1:p.Val3128=
XM_017009972.1:c.2500G=	XP_016865461.1:p.Val834=
XM_017009973.1:c.2479G=	XP_016865462.1:p.Val827=
XM_017009974.2:c.9382G=	XP_016865463.1:p.Val3128=
XR_001742802.1:n.2523-834C=
NR_003149.2:n.9377G=