Canonical Allele Identifier: CA2674577101

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90823504-CTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823508_90823510del , CM000667.2:g.90823508_90823510del	GRCh38
NC_000005.9:g.90119325_90119327del , CM000667.1:g.90119325_90119327del	GRCh37
NC_000005.8:g.90155081_90155083del	NCBI36
NG_007083.1:g.269709_269711del
NG_007083.2:g.299165_299167del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16280_16282del MANE Select	ENSP00000384582.2:p.Val5427del
ENST00000425867.3:c.5234_5236del	ENSP00000392618.3:p.Val1745del
ENST00000638510.1:n.3547_3549del
ENST00000639431.1:c.265+147299_265+147301del	ENSP00000491057.1:n.265+147299_265+147301del
ENST00000640061.1:n.128+1326_128+1328del
ENST00000640407.1:c.2690_2692del	ENSP00000491425.1:p.Val897del
ENST00000405460.6:c.16280_16282del	ENSP00000384582.2:p.Val5427del
ENST00000425867.2:c.3263_3265del	ENSP00000392618.2:p.Val1088del
NM_032119.3:c.16280_16282del	NP_115495.3:p.Val5427del
NR_003149.1:n.16293_16295del
XM_011543675.1:c.16277_16279del	XP_011541977.1:p.Val5426del
XM_011543676.1:c.16199_16201del	XP_011541978.1:p.Val5400del
XM_011543677.1:c.13583_13585del	XP_011541979.1:p.Val4528del
NM_032119.4:c.16280_16282del MANE Select	NP_115495.3:p.Val5427del
XM_017009963.2:c.16301_16303del	XP_016865452.1:p.Val5434del
XM_017009964.2:c.16298_16300del	XP_016865453.1:p.Val5433del
XM_017009965.1:c.16298_16300del	XP_016865454.1:p.Val5433del
XM_017009966.2:c.16220_16222del	XP_016865455.1:p.Val5407del
XM_017009967.1:c.16205_16207del	XP_016865456.1:p.Val5402del
XM_017009968.2:c.16121_16123del	XP_016865457.1:p.Val5374del
XM_017009969.2:c.16301_16303del	XP_016865458.1:p.Val5434del
XM_017009972.1:c.9419_9421del	XP_016865461.1:p.Val3140del
XM_017009973.1:c.9398_9400del	XP_016865462.1:p.Val3133del
NR_003149.2:n.16296_16298del