Canonical Allele Identifier: CA1562870621

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716658T= , CM000667.2:g.90716658T=	GRCh38
NC_000005.9:g.90012475T= , CM000667.1:g.90012475T=	GRCh37
NC_000005.8:g.90048231T=	NCBI36
NG_007083.1:g.162859T=
NG_007083.2:g.192315T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9376T= MANE Select	ENSP00000384582.2:p.Ser3126=
ENST00000639431.1:c.265+40449T=	ENSP00000491057.1:n.265+40449T=
ENST00000639473.1:n.4835T=
ENST00000640012.1:c.3183T=
ENST00000640374.1:n.2520T=
ENST00000640779.1:c.4105T=
ENST00000405460.6:c.9376T=	ENSP00000384582.2:p.Ser3126=
ENST00000509621.1:c.2073T=
NM_032119.3:c.9376T=	NP_115495.3:p.Ser3126=
NR_003149.1:n.9389T=
XM_011543675.1:c.9373T=	XP_011541977.1:p.Ser3125=
XM_011543676.1:c.9295T=	XP_011541978.1:p.Ser3099=
XM_011543677.1:c.6679T=	XP_011541979.1:p.Ser2227=
XM_011543678.1:c.9376T=	XP_011541980.1:p.Ser3126=
XM_011543679.1:c.9376T=	XP_011541981.1:p.Ser3126=
XR_948560.1:n.272-849A=
NM_032119.4:c.9376T= MANE Select	NP_115495.3:p.Ser3126=
XM_017009963.2:c.9397T=	XP_016865452.1:p.Ser3133=
XM_017009964.2:c.9394T=	XP_016865453.1:p.Ser3132=
XM_017009965.1:c.9394T=	XP_016865454.1:p.Ser3132=
XM_017009966.2:c.9316T=	XP_016865455.1:p.Ser3106=
XM_017009967.1:c.9301T=	XP_016865456.1:p.Ser3101=
XM_017009968.2:c.9397T=	XP_016865457.1:p.Ser3133=
XM_017009969.2:c.9397T=	XP_016865458.1:p.Ser3133=
XM_017009970.2:c.9397T=	XP_016865459.1:p.Ser3133=
XM_017009971.2:c.9397T=	XP_016865460.1:p.Ser3133=
XM_017009972.1:c.2515T=	XP_016865461.1:p.Ser839=
XM_017009973.1:c.2494T=	XP_016865462.1:p.Ser832=
XM_017009974.2:c.9397T=	XP_016865463.1:p.Ser3133=
XR_001742802.1:n.2523-849A=
NR_003149.2:n.9392T=