Canonical Allele Identifier: CA1562886198

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755086T= , CM000667.2:g.90755086T=	GRCh38
NC_000005.9:g.90050903T= , CM000667.1:g.90050903T=	GRCh37
NC_000005.8:g.90086659T=	NCBI36
NG_007083.1:g.201287T=
NG_007083.2:g.230743T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11481T= MANE Select	ENSP00000384582.2:p.Asp3827=
ENST00000425867.3:c.612T=	ENSP00000392618.3:p.Asp204=
ENST00000639431.1:c.265+78877T=	ENSP00000491057.1:n.265+78877T=
ENST00000640374.1:n.4625T=
ENST00000640464.1:n.1900T=
ENST00000405460.6:c.11481T=	ENSP00000384582.2:p.Asp3827=
ENST00000509621.1:c.4178T=
NM_032119.3:c.11481T=	NP_115495.3:p.Asp3827=
NR_003149.1:n.11494T=
XM_011543675.1:c.11478T=	XP_011541977.1:p.Asp3826=
XM_011543676.1:c.11400T=	XP_011541978.1:p.Asp3800=
XM_011543677.1:c.8784T=	XP_011541979.1:p.Asp2928=
XM_011543678.1:c.11481T=	XP_011541980.1:p.Asp3827=
NM_032119.4:c.11481T= MANE Select	NP_115495.3:p.Asp3827=
XM_017009963.2:c.11502T=	XP_016865452.1:p.Asp3834=
XM_017009964.2:c.11499T=	XP_016865453.1:p.Asp3833=
XM_017009965.1:c.11499T=	XP_016865454.1:p.Asp3833=
XM_017009966.2:c.11421T=	XP_016865455.1:p.Asp3807=
XM_017009967.1:c.11406T=	XP_016865456.1:p.Asp3802=
XM_017009968.2:c.11502T=	XP_016865457.1:p.Asp3834=
XM_017009969.2:c.11502T=	XP_016865458.1:p.Asp3834=
XM_017009970.2:c.11502T=	XP_016865459.1:p.Asp3834=
XM_017009971.2:c.11502T=	XP_016865460.1:p.Asp3834=
XM_017009972.1:c.4620T=	XP_016865461.1:p.Asp1540=
XM_017009973.1:c.4599T=	XP_016865462.1:p.Asp1533=
NR_003149.2:n.11497T=