Canonical Allele Identifier: CA360367091

Gene: ADGRV1

Linked Data

• ClinVar Variation Id: 1927744
• ClinVar RCV Id: RCV002610038
• dbSNP Id: rs779442763
• gnomAD v4: 5-90627499-G-A
• MyVariant Identifiers: chr5:g.89923316G>A (hg19) ; chr5:g.90627499G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90627499G>A , CM000667.2:g.90627499G>A	GRCh38
NC_000005.9:g.89923316G>A , CM000667.1:g.89923316G>A	GRCh37
NC_000005.8:g.89959072G>A	NCBI36
NG_007083.1:g.73700G>A
NG_007083.2:g.103156G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.961G>A MANE Select	ENSP00000384582.2:p.Asp321Asn
ENST00000640083.1:n.666G>A
ENST00000640109.1:n.1057G>A
ENST00000640281.1:n.1020G>A
ENST00000405460.6:c.961G>A	ENSP00000384582.2:p.Asp321Asn
NM_032119.3:c.961G>A	NP_115495.3:p.Asp321Asn
NR_003149.1:n.1057G>A
XM_011543675.1:c.961G>A	XP_011541977.1:p.Asp321Asn
XM_011543676.1:c.961G>A	XP_011541978.1:p.Asp321Asn
XM_011543678.1:c.961G>A	XP_011541980.1:p.Asp321Asn
XM_011543679.1:c.961G>A	XP_011541981.1:p.Asp321Asn
NM_032119.4:c.961G>A MANE Select	NP_115495.3:p.Asp321Asn
XM_017009963.2:c.961G>A	XP_016865452.1:p.Asp321Asn
XM_017009964.2:c.961G>A	XP_016865453.1:p.Asp321Asn
XM_017009965.1:c.958G>A	XP_016865454.1:p.Asp320Asn
XM_017009966.2:c.961G>A	XP_016865455.1:p.Asp321Asn
XM_017009967.1:c.865G>A	XP_016865456.1:p.Asp289Asn
XM_017009968.2:c.961G>A	XP_016865457.1:p.Asp321Asn
XM_017009969.2:c.961G>A	XP_016865458.1:p.Asp321Asn
XM_017009970.2:c.961G>A	XP_016865459.1:p.Asp321Asn
XM_017009971.2:c.961G>A	XP_016865460.1:p.Asp321Asn
XM_017009974.2:c.961G>A	XP_016865463.1:p.Asp321Asn
NR_003149.2:n.1060G>A