Canonical Allele Identifier: CA360396233

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712341-G-A
• MyVariant Identifiers: chr5:g.90008158G>A (hg19) ; chr5:g.90712341G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712341G>A , CM000667.2:g.90712341G>A	GRCh38
NC_000005.9:g.90008158G>A , CM000667.1:g.90008158G>A	GRCh37
NC_000005.8:g.90043914G>A	NCBI36
NG_007083.1:g.158542G>A
NG_007083.2:g.187998G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9097G>A MANE Select	ENSP00000384582.2:p.Asp3033Asn
ENST00000639431.1:c.265+36132G>A	ENSP00000491057.1:n.265+36132G>A
ENST00000639473.1:n.4556G>A
ENST00000640012.1:c.2904G>A
ENST00000640374.1:n.2241G>A
ENST00000640779.1:c.3826G>A
ENST00000405460.6:c.9097G>A	ENSP00000384582.2:p.Asp3033Asn
ENST00000509621.1:c.1794G>A
NM_032119.3:c.9097G>A	NP_115495.3:p.Asp3033Asn
NR_003149.1:n.9110G>A
XM_011543675.1:c.9094G>A	XP_011541977.1:p.Asp3032Asn
XM_011543676.1:c.9016G>A	XP_011541978.1:p.Asp3006Asn
XM_011543677.1:c.6400G>A	XP_011541979.1:p.Asp2134Asn
XM_011543678.1:c.9097G>A	XP_011541980.1:p.Asp3033Asn
XM_011543679.1:c.9097G>A	XP_011541981.1:p.Asp3033Asn
NM_032119.4:c.9097G>A MANE Select	NP_115495.3:p.Asp3033Asn
XM_017009963.2:c.9118G>A	XP_016865452.1:p.Asp3040Asn
XM_017009964.2:c.9115G>A	XP_016865453.1:p.Asp3039Asn
XM_017009965.1:c.9115G>A	XP_016865454.1:p.Asp3039Asn
XM_017009966.2:c.9037G>A	XP_016865455.1:p.Asp3013Asn
XM_017009967.1:c.9022G>A	XP_016865456.1:p.Asp3008Asn
XM_017009968.2:c.9118G>A	XP_016865457.1:p.Asp3040Asn
XM_017009969.2:c.9118G>A	XP_016865458.1:p.Asp3040Asn
XM_017009970.2:c.9118G>A	XP_016865459.1:p.Asp3040Asn
XM_017009971.2:c.9118G>A	XP_016865460.1:p.Asp3040Asn
XM_017009972.1:c.2236G>A	XP_016865461.1:p.Asp746Asn
XM_017009973.1:c.2215G>A	XP_016865462.1:p.Asp739Asn
XM_017009974.2:c.9118G>A	XP_016865463.1:p.Asp3040Asn
NR_003149.2:n.9113G>A