Canonical Allele Identifier: CA1562870622

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716662C= , CM000667.2:g.90716662C=	GRCh38
NC_000005.9:g.90012479C= , CM000667.1:g.90012479C=	GRCh37
NC_000005.8:g.90048235C=	NCBI36
NG_007083.1:g.162863C=
NG_007083.2:g.192319C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9380C= MANE Select	ENSP00000384582.2:p.Ser3127=
ENST00000639431.1:c.265+40453C=	ENSP00000491057.1:n.265+40453C=
ENST00000639473.1:n.4839C=
ENST00000640012.1:c.3187C=
ENST00000640374.1:n.2524C=
ENST00000640779.1:c.4109C=
ENST00000405460.6:c.9380C=	ENSP00000384582.2:p.Ser3127=
ENST00000509621.1:c.2077C=
NM_032119.3:c.9380C=	NP_115495.3:p.Ser3127=
NR_003149.1:n.9393C=
XM_011543675.1:c.9377C=	XP_011541977.1:p.Ser3126=
XM_011543676.1:c.9299C=	XP_011541978.1:p.Ser3100=
XM_011543677.1:c.6683C=	XP_011541979.1:p.Ser2228=
XM_011543678.1:c.9380C=	XP_011541980.1:p.Ser3127=
XM_011543679.1:c.9380C=	XP_011541981.1:p.Ser3127=
XR_948560.1:n.272-853G=
NM_032119.4:c.9380C= MANE Select	NP_115495.3:p.Ser3127=
XM_017009963.2:c.9401C=	XP_016865452.1:p.Ser3134=
XM_017009964.2:c.9398C=	XP_016865453.1:p.Ser3133=
XM_017009965.1:c.9398C=	XP_016865454.1:p.Ser3133=
XM_017009966.2:c.9320C=	XP_016865455.1:p.Ser3107=
XM_017009967.1:c.9305C=	XP_016865456.1:p.Ser3102=
XM_017009968.2:c.9401C=	XP_016865457.1:p.Ser3134=
XM_017009969.2:c.9401C=	XP_016865458.1:p.Ser3134=
XM_017009970.2:c.9401C=	XP_016865459.1:p.Ser3134=
XM_017009971.2:c.9401C=	XP_016865460.1:p.Ser3134=
XM_017009972.1:c.2519C=	XP_016865461.1:p.Ser840=
XM_017009973.1:c.2498C=	XP_016865462.1:p.Ser833=
XM_017009974.2:c.9401C=	XP_016865463.1:p.Ser3134=
XR_001742802.1:n.2523-853G=
NR_003149.2:n.9396C=