Canonical Allele Identifier: CA2674570022

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712301-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712302del , CM000667.2:g.90712302del	GRCh38
NC_000005.9:g.90008119del , CM000667.1:g.90008119del	GRCh37
NC_000005.8:g.90043875del	NCBI36
NG_007083.1:g.158503del
NG_007083.2:g.187959del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9058del MANE Select	ENSP00000384582.2:p.Asp3020MetfsTer11
ENST00000639431.1:c.265+36093del	ENSP00000491057.1:n.265+36093del
ENST00000639473.1:n.4517del
ENST00000640012.1:c.2865del
ENST00000640374.1:n.2202del
ENST00000640779.1:c.3787del
ENST00000405460.6:c.9058del	ENSP00000384582.2:p.Asp3020MetfsTer11
ENST00000509621.1:c.1755del
NM_032119.3:c.9058del	NP_115495.3:p.Asp3020MetfsTer11
NR_003149.1:n.9071del
XM_011543675.1:c.9055del	XP_011541977.1:p.Asp3019MetfsTer11
XM_011543676.1:c.8977del	XP_011541978.1:p.Asp2993MetfsTer11
XM_011543677.1:c.6361del	XP_011541979.1:p.Asp2121MetfsTer11
XM_011543678.1:c.9058del	XP_011541980.1:p.Asp3020MetfsTer11
XM_011543679.1:c.9058del	XP_011541981.1:p.Asp3020MetfsTer11
NM_032119.4:c.9058del MANE Select	NP_115495.3:p.Asp3020MetfsTer11
XM_017009963.2:c.9079del	XP_016865452.1:p.Asp3027MetfsTer11
XM_017009964.2:c.9076del	XP_016865453.1:p.Asp3026MetfsTer11
XM_017009965.1:c.9076del	XP_016865454.1:p.Asp3026MetfsTer11
XM_017009966.2:c.8998del	XP_016865455.1:p.Asp3000MetfsTer11
XM_017009967.1:c.8983del	XP_016865456.1:p.Asp2995MetfsTer11
XM_017009968.2:c.9079del	XP_016865457.1:p.Asp3027MetfsTer11
XM_017009969.2:c.9079del	XP_016865458.1:p.Asp3027MetfsTer11
XM_017009970.2:c.9079del	XP_016865459.1:p.Asp3027MetfsTer11
XM_017009971.2:c.9079del	XP_016865460.1:p.Asp3027MetfsTer11
XM_017009972.1:c.2197del	XP_016865461.1:p.Asp733MetfsTer11
XM_017009973.1:c.2176del	XP_016865462.1:p.Asp726MetfsTer11
XM_017009974.2:c.9079del	XP_016865463.1:p.Asp3027MetfsTer11
NR_003149.2:n.9074del