Canonical Allele Identifier: CA815356148

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1263883168
• gnomAD v3: 5-90763163-AT-A
• gnomAD v4: 5-90763163-AT-A
• MyVariant Identifiers: chr5:g.90058981del (hg19) ; chr5:g.90763164del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763168del , CM000667.2:g.90763168del	GRCh38
NC_000005.9:g.90058985del , CM000667.1:g.90058985del	GRCh37
NC_000005.8:g.90094741del	NCBI36
NG_007083.1:g.209369del
NG_007083.2:g.238825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12121-137del MANE Select	ENSP00000384582.2:n.12121-137del
ENST00000425867.3:c.1075-137del	ENSP00000392618.3:n.1075-137del
ENST00000639431.1:c.265+86959del	ENSP00000491057.1:n.265+86959del
ENST00000640464.1:n.2540-137del
ENST00000640729.1:n.561del
ENST00000405460.6:c.12121-137del	ENSP00000384582.2:n.12121-137del
NM_032119.3:c.12121-137del	NP_115495.3:n.12121-137del
NR_003149.1:n.12134-137del
XM_011543675.1:c.12118-137del	XP_011541977.1:n.12118-137del
XM_011543676.1:c.12040-137del	XP_011541978.1:n.12040-137del
XM_011543677.1:c.9424-137del	XP_011541979.1:n.9424-137del
XM_011543678.1:c.12121-137del	XP_011541980.1:n.12121-137del
NM_032119.4:c.12121-137del MANE Select	NP_115495.3:n.12121-137del
XM_017009963.2:c.12142-137del	XP_016865452.1:n.12142-137del
XM_017009964.2:c.12139-137del	XP_016865453.1:n.12139-137del
XM_017009965.1:c.12139-137del	XP_016865454.1:n.12139-137del
XM_017009966.2:c.12061-137del	XP_016865455.1:n.12061-137del
XM_017009967.1:c.12046-137del	XP_016865456.1:n.12046-137del
XM_017009968.2:c.12142-137del	XP_016865457.1:n.12142-137del
XM_017009969.2:c.12142-137del	XP_016865458.1:n.12142-137del
XM_017009970.2:c.12142-137del	XP_016865459.1:n.12142-137del
XM_017009971.2:c.12142-137del	XP_016865460.1:n.12142-137del
XM_017009972.1:c.5260-137del	XP_016865461.1:n.5260-137del
XM_017009973.1:c.5239-137del	XP_016865462.1:n.5239-137del
NR_003149.2:n.12137-137del