Canonical Allele Identifier: CA3341144

Gene: ADGRV1

Linked Data

• dbSNP Id: rs549879061
• ExAC: 5:90059083 T / TC
• gnomAD v2: 5-90059083-T-TC
• gnomAD v3: 5-90763266-T-TC
• gnomAD v4: 5-90763266-T-TC
• MyVariant Identifiers: chr5:g.90059083_90059084insC (hg19) ; chr5:g.90763266_90763267insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90763266_90763267insC , CM000667.2:g.90763266_90763267insC	GRCh38
NC_000005.9:g.90059083_90059084insC , CM000667.1:g.90059083_90059084insC	GRCh37
NC_000005.8:g.90094839_90094840insC	NCBI36
NG_007083.1:g.209467_209468insC
NG_007083.2:g.238923_238924insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.12121-39_12121-38insC MANE Select	ENSP00000384582.2:n.12121-39_12121-38insC
ENST00000425867.3:c.1075-39_1075-38insC	ENSP00000392618.3:n.1075-39_1075-38insC
ENST00000639431.1:c.265+87057_265+87058insC	ENSP00000491057.1:n.265+87057_265+87058insC
ENST00000640464.1:n.2540-39_2540-38insC
ENST00000640729.1:n.659_660insC
ENST00000405460.6:c.12121-39_12121-38insC	ENSP00000384582.2:n.12121-39_12121-38insC
NM_032119.3:c.12121-39_12121-38insC	NP_115495.3:n.12121-39_12121-38insC
NR_003149.1:n.12134-39_12134-38insC
XM_011543675.1:c.12118-39_12118-38insC	XP_011541977.1:n.12118-39_12118-38insC
XM_011543676.1:c.12040-39_12040-38insC	XP_011541978.1:n.12040-39_12040-38insC
XM_011543677.1:c.9424-39_9424-38insC	XP_011541979.1:n.9424-39_9424-38insC
XM_011543678.1:c.12121-39_12121-38insC	XP_011541980.1:n.12121-39_12121-38insC
NM_032119.4:c.12121-39_12121-38insC MANE Select	NP_115495.3:n.12121-39_12121-38insC
XM_017009963.2:c.12142-39_12142-38insC	XP_016865452.1:n.12142-39_12142-38insC
XM_017009964.2:c.12139-39_12139-38insC	XP_016865453.1:n.12139-39_12139-38insC
XM_017009965.1:c.12139-39_12139-38insC	XP_016865454.1:n.12139-39_12139-38insC
XM_017009966.2:c.12061-39_12061-38insC	XP_016865455.1:n.12061-39_12061-38insC
XM_017009967.1:c.12046-39_12046-38insC	XP_016865456.1:n.12046-39_12046-38insC
XM_017009968.2:c.12142-39_12142-38insC	XP_016865457.1:n.12142-39_12142-38insC
XM_017009969.2:c.12142-39_12142-38insC	XP_016865458.1:n.12142-39_12142-38insC
XM_017009970.2:c.12142-39_12142-38insC	XP_016865459.1:n.12142-39_12142-38insC
XM_017009971.2:c.12142-39_12142-38insC	XP_016865460.1:n.12142-39_12142-38insC
XM_017009972.1:c.5260-39_5260-38insC	XP_016865461.1:n.5260-39_5260-38insC
XM_017009973.1:c.5239-39_5239-38insC	XP_016865462.1:n.5239-39_5239-38insC
NR_003149.2:n.12137-39_12137-38insC