Canonical Allele Identifier: CA1562881838

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745076C= , CM000667.2:g.90745076C=	GRCh38
NC_000005.9:g.90040893C= , CM000667.1:g.90040893C=	GRCh37
NC_000005.8:g.90076649C=	NCBI36
NG_007083.1:g.191277C=
NG_007083.2:g.220733C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10580C= MANE Select	ENSP00000384582.2:p.Ser3527=
ENST00000639431.1:c.265+68867C=	ENSP00000491057.1:n.265+68867C=
ENST00000640374.1:n.3724C=
ENST00000640464.1:n.999C=
ENST00000405460.6:c.10580C=	ENSP00000384582.2:p.Ser3527=
ENST00000509621.1:c.3277C=
NM_032119.3:c.10580C=	NP_115495.3:p.Ser3527=
NR_003149.1:n.10593C=
XM_011543675.1:c.10577C=	XP_011541977.1:p.Ser3526=
XM_011543676.1:c.10499C=	XP_011541978.1:p.Ser3500=
XM_011543677.1:c.7883C=	XP_011541979.1:p.Ser2628=
XM_011543678.1:c.10580C=	XP_011541980.1:p.Ser3527=
XM_011543679.1:c.10580C=	XP_011541981.1:p.Ser3527=
NM_032119.4:c.10580C= MANE Select	NP_115495.3:p.Ser3527=
XM_017009963.2:c.10601C=	XP_016865452.1:p.Ser3534=
XM_017009964.2:c.10598C=	XP_016865453.1:p.Ser3533=
XM_017009965.1:c.10598C=	XP_016865454.1:p.Ser3533=
XM_017009966.2:c.10520C=	XP_016865455.1:p.Ser3507=
XM_017009967.1:c.10505C=	XP_016865456.1:p.Ser3502=
XM_017009968.2:c.10601C=	XP_016865457.1:p.Ser3534=
XM_017009969.2:c.10601C=	XP_016865458.1:p.Ser3534=
XM_017009970.2:c.10601C=	XP_016865459.1:p.Ser3534=
XM_017009971.2:c.10601C=	XP_016865460.1:p.Ser3534=
XM_017009972.1:c.3719C=	XP_016865461.1:p.Ser1240=
XM_017009973.1:c.3698C=	XP_016865462.1:p.Ser1233=
XM_017009974.2:c.10601C=	XP_016865463.1:p.Ser3534=
NR_003149.2:n.10596C=