Canonical Allele Identifier: CA1562886199

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755086_90755090delinsTAATC , CM000667.2:g.90755086_90755090delinsTAATC	GRCh38
NC_000005.9:g.90050903_90050907delinsTAATC , CM000667.1:g.90050903_90050907delinsTAATC	GRCh37
NC_000005.8:g.90086659_90086663delinsTAATC	NCBI36
NG_007083.1:g.201287_201291delinsTAATC
NG_007083.2:g.230743_230747delinsTAATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11481_11485delinsTAATC MANE Select	ENSP00000384582.2:p.Asp3827=
ENST00000425867.3:c.612_616delinsTAATC	ENSP00000392618.3:p.Asp204=
ENST00000639431.1:c.265+78877_265+78881delinsTAATC	ENSP00000491057.1:n.265+78877_265+78881de...
ENST00000640374.1:n.4625_4629delinsTAATC
ENST00000640464.1:n.1900_1904delinsTAATC
ENST00000405460.6:c.11481_11485delinsTAATC	ENSP00000384582.2:p.Asp3827=
ENST00000509621.1:c.4178_4182delinsTAATC
NM_032119.3:c.11481_11485delinsTAATC	NP_115495.3:p.Asp3827=
NR_003149.1:n.11494_11498delinsTAATC
XM_011543675.1:c.11478_11482delinsTAATC	XP_011541977.1:p.Asp3826=
XM_011543676.1:c.11400_11404delinsTAATC	XP_011541978.1:p.Asp3800=
XM_011543677.1:c.8784_8788delinsTAATC	XP_011541979.1:p.Asp2928=
XM_011543678.1:c.11481_11485delinsTAATC	XP_011541980.1:p.Asp3827=
NM_032119.4:c.11481_11485delinsTAATC MANE Select	NP_115495.3:p.Asp3827=
XM_017009963.2:c.11502_11506delinsTAATC	XP_016865452.1:p.Asp3834=
XM_017009964.2:c.11499_11503delinsTAATC	XP_016865453.1:p.Asp3833=
XM_017009965.1:c.11499_11503delinsTAATC	XP_016865454.1:p.Asp3833=
XM_017009966.2:c.11421_11425delinsTAATC	XP_016865455.1:p.Asp3807=
XM_017009967.1:c.11406_11410delinsTAATC	XP_016865456.1:p.Asp3802=
XM_017009968.2:c.11502_11506delinsTAATC	XP_016865457.1:p.Asp3834=
XM_017009969.2:c.11502_11506delinsTAATC	XP_016865458.1:p.Asp3834=
XM_017009970.2:c.11502_11506delinsTAATC	XP_016865459.1:p.Asp3834=
XM_017009971.2:c.11502_11506delinsTAATC	XP_016865460.1:p.Asp3834=
XM_017009972.1:c.4620_4624delinsTAATC	XP_016865461.1:p.Asp1540=
XM_017009973.1:c.4599_4603delinsTAATC	XP_016865462.1:p.Asp1533=
NR_003149.2:n.11497_11501delinsTAATC