Canonical Allele Identifier: CA2674560118

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90617833-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90617834del , CM000667.2:g.90617834del	GRCh38
NC_000005.9:g.89913651del , CM000667.1:g.89913651del	GRCh37
NC_000005.8:g.89949407del	NCBI36
NG_007083.1:g.64035del
NG_007083.2:g.93491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.238del MANE Select	ENSP00000384582.2:p.Asp80ThrfsTer19
ENST00000638316.1:n.448del
ENST00000638638.1:n.645del
ENST00000640109.1:n.334del
ENST00000640281.1:n.297del
ENST00000405460.6:c.238del	ENSP00000384582.2:p.Asp80ThrfsTer19
ENST00000508842.5:c.250del	ENSP00000425936.1:p.Asp84ThrfsTer19
NM_032119.3:c.238del	NP_115495.3:p.Asp80ThrfsTer19
NR_003149.1:n.334del
XM_011543675.1:c.238del	XP_011541977.1:p.Asp80ThrfsTer19
XM_011543676.1:c.238del	XP_011541978.1:p.Asp80ThrfsTer19
XM_011543678.1:c.238del	XP_011541980.1:p.Asp80ThrfsTer19
XM_011543679.1:c.238del	XP_011541981.1:p.Asp80ThrfsTer19
NM_032119.4:c.238del MANE Select	NP_115495.3:p.Asp80ThrfsTer19
XM_017009963.2:c.238del	XP_016865452.1:p.Asp80ThrfsTer19
XM_017009964.2:c.238del	XP_016865453.1:p.Asp80ThrfsTer19
XM_017009965.1:c.235del	XP_016865454.1:p.Asp79ThrfsTer19
XM_017009966.2:c.238del	XP_016865455.1:p.Asp80ThrfsTer19
XM_017009967.1:c.238del	XP_016865456.1:p.Asp80ThrfsTer19
XM_017009968.2:c.238del	XP_016865457.1:p.Asp80ThrfsTer19
XM_017009969.2:c.238del	XP_016865458.1:p.Asp80ThrfsTer19
XM_017009970.2:c.238del	XP_016865459.1:p.Asp80ThrfsTer19
XM_017009971.2:c.238del	XP_016865460.1:p.Asp80ThrfsTer19
XM_017009974.2:c.238del	XP_016865463.1:p.Asp80ThrfsTer19
NR_003149.2:n.337del