Canonical Allele Identifier: CA1562867548

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712378T= , CM000667.2:g.90712378T=	GRCh38
NC_000005.9:g.90008195T= , CM000667.1:g.90008195T=	GRCh37
NC_000005.8:g.90043951T=	NCBI36
NG_007083.1:g.158579T=
NG_007083.2:g.188035T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9134T= MANE Select	ENSP00000384582.2:p.Leu3045=
ENST00000639431.1:c.265+36169T=	ENSP00000491057.1:n.265+36169T=
ENST00000639473.1:n.4593T=
ENST00000640012.1:c.2941T=
ENST00000640374.1:n.2278T=
ENST00000640779.1:c.3863T=
ENST00000405460.6:c.9134T=	ENSP00000384582.2:p.Leu3045=
ENST00000509621.1:c.1831T=
NM_032119.3:c.9134T=	NP_115495.3:p.Leu3045=
NR_003149.1:n.9147T=
XM_011543675.1:c.9131T=	XP_011541977.1:p.Leu3044=
XM_011543676.1:c.9053T=	XP_011541978.1:p.Leu3018=
XM_011543677.1:c.6437T=	XP_011541979.1:p.Leu2146=
XM_011543678.1:c.9134T=	XP_011541980.1:p.Leu3045=
XM_011543679.1:c.9134T=	XP_011541981.1:p.Leu3045=
XR_948560.1:n.468A=
NM_032119.4:c.9134T= MANE Select	NP_115495.3:p.Leu3045=
XM_017009963.2:c.9155T=	XP_016865452.1:p.Leu3052=
XM_017009964.2:c.9152T=	XP_016865453.1:p.Leu3051=
XM_017009965.1:c.9152T=	XP_016865454.1:p.Leu3051=
XM_017009966.2:c.9074T=	XP_016865455.1:p.Leu3025=
XM_017009967.1:c.9059T=	XP_016865456.1:p.Leu3020=
XM_017009968.2:c.9155T=	XP_016865457.1:p.Leu3052=
XM_017009969.2:c.9155T=	XP_016865458.1:p.Leu3052=
XM_017009970.2:c.9155T=	XP_016865459.1:p.Leu3052=
XM_017009971.2:c.9155T=	XP_016865460.1:p.Leu3052=
XM_017009972.1:c.2273T=	XP_016865461.1:p.Leu758=
XM_017009973.1:c.2252T=	XP_016865462.1:p.Leu751=
XM_017009974.2:c.9155T=	XP_016865463.1:p.Leu3052=
NR_003149.2:n.9150T=