Canonical Allele Identifier: CA2578359687

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755098_90755099del , CM000667.2:g.90755098_90755099del	GRCh38
NC_000005.9:g.90050915_90050916del , CM000667.1:g.90050915_90050916del	GRCh37
NC_000005.8:g.90086671_90086672del	NCBI36
NG_007083.1:g.201299_201300del
NG_007083.2:g.230755_230756del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11493_11494del MANE Select	ENSP00000384582.2:p.Asn3833Ter
ENST00000425867.3:c.624_625del	ENSP00000392618.3:p.Asn210Ter
ENST00000639431.1:c.265+78889_265+78890del	ENSP00000491057.1:n.265+78889_265+78890del
ENST00000640374.1:n.4637_4638del
ENST00000640464.1:n.1912_1913del
ENST00000405460.6:c.11493_11494del	ENSP00000384582.2:p.Asn3833Ter
ENST00000509621.1:c.4190_4191del
NM_032119.3:c.11493_11494del	NP_115495.3:p.Asn3833Ter
NR_003149.1:n.11506_11507del
XM_011543675.1:c.11490_11491del	XP_011541977.1:p.Asn3832Ter
XM_011543676.1:c.11412_11413del	XP_011541978.1:p.Asn3806Ter
XM_011543677.1:c.8796_8797del	XP_011541979.1:p.Asn2934Ter
XM_011543678.1:c.11493_11494del	XP_011541980.1:p.Asn3833Ter
NM_032119.4:c.11493_11494del MANE Select	NP_115495.3:p.Asn3833Ter
XM_017009963.2:c.11514_11515del	XP_016865452.1:p.Asn3840Ter
XM_017009964.2:c.11511_11512del	XP_016865453.1:p.Asn3839Ter
XM_017009965.1:c.11511_11512del	XP_016865454.1:p.Asn3839Ter
XM_017009966.2:c.11433_11434del	XP_016865455.1:p.Asn3813Ter
XM_017009967.1:c.11418_11419del	XP_016865456.1:p.Asn3808Ter
XM_017009968.2:c.11514_11515del	XP_016865457.1:p.Asn3840Ter
XM_017009969.2:c.11514_11515del	XP_016865458.1:p.Asn3840Ter
XM_017009970.2:c.11514_11515del	XP_016865459.1:p.Asn3840Ter
XM_017009971.2:c.11514_11515del	XP_016865460.1:p.Asn3840Ter
XM_017009972.1:c.4632_4633del	XP_016865461.1:p.Asn1546Ter
XM_017009973.1:c.4611_4612del	XP_016865462.1:p.Asn1539Ter
NR_003149.2:n.11509_11510del