Canonical Allele Identifier: CA1562882060

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745603G= , CM000667.2:g.90745603G=	GRCh38
NC_000005.9:g.90041420G= , CM000667.1:g.90041420G=	GRCh37
NC_000005.8:g.90077176G=	NCBI36
NG_007083.1:g.191804G=
NG_007083.2:g.221260G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10782G= MANE Select	ENSP00000384582.2:p.Leu3594=
ENST00000639431.1:c.265+69394G=	ENSP00000491057.1:n.265+69394G=
ENST00000640374.1:n.3926G=
ENST00000640464.1:n.1201G=
ENST00000405460.6:c.10782G=	ENSP00000384582.2:p.Leu3594=
ENST00000509621.1:c.3479G=
NM_032119.3:c.10782G=	NP_115495.3:p.Leu3594=
NR_003149.1:n.10795G=
XM_011543675.1:c.10779G=	XP_011541977.1:p.Leu3593=
XM_011543676.1:c.10701G=	XP_011541978.1:p.Leu3567=
XM_011543677.1:c.8085G=	XP_011541979.1:p.Leu2695=
XM_011543678.1:c.10782G=	XP_011541980.1:p.Leu3594=
XM_011543679.1:c.*4G=	XP_011541981.1:n.*4G=
NM_032119.4:c.10782G= MANE Select	NP_115495.3:p.Leu3594=
XM_017009963.2:c.10803G=	XP_016865452.1:p.Leu3601=
XM_017009964.2:c.10800G=	XP_016865453.1:p.Leu3600=
XM_017009965.1:c.10800G=	XP_016865454.1:p.Leu3600=
XM_017009966.2:c.10722G=	XP_016865455.1:p.Leu3574=
XM_017009967.1:c.10707G=	XP_016865456.1:p.Leu3569=
XM_017009968.2:c.10803G=	XP_016865457.1:p.Leu3601=
XM_017009969.2:c.10803G=	XP_016865458.1:p.Leu3601=
XM_017009970.2:c.10803G=	XP_016865459.1:p.Leu3601=
XM_017009971.2:c.10803G=	XP_016865460.1:p.Leu3601=
XM_017009972.1:c.3921G=	XP_016865461.1:p.Leu1307=
XM_017009973.1:c.3900G=	XP_016865462.1:p.Leu1300=
XM_017009974.2:c.*4G=	XP_016865463.1:n.*4G=
NR_003149.2:n.10798G=