Canonical Allele Identifier: CA3338519
Community Standard Title: NM_032119.4(ADGRV1):c.664G>A (p.Asp222Asn)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90625235G>A , CM000667.2:g.90625235G>A GRCh38
NC_000005.9:g.89921052G>A , CM000667.1:g.89921052G>A GRCh37
NC_000005.8:g.89956808G>A NCBI36
NG_007083.1:g.71436G>A
NG_007083.2:g.100892G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.664G>A MANE Select NP_115495.3:p.Asp222Asn
ENST00000405460.9:c.664G>A MANE Select ENSP00000384582.2:p.Asp222Asn
NM_032119.3:c.664G>A NP_115495.3:p.Asp222Asn
NR_003149.1:n.760G>A
NR_003149.2:n.763G>A
ENST00000405460.6:c.664G>A ENSP00000384582.2:p.Asp222Asn
ENST00000638316.1:n.874G>A
ENST00000638638.1:n.1071G>A
ENST00000640083.1:n.369G>A
ENST00000640109.1:n.760G>A
ENST00000640281.1:n.723G>A
XM_011543675.1:c.664G>A XP_011541977.1:p.Asp222Asn
XM_011543676.1:c.664G>A XP_011541978.1:p.Asp222Asn
XM_011543678.1:c.664G>A XP_011541980.1:p.Asp222Asn
XM_011543679.1:c.664G>A XP_011541981.1:p.Asp222Asn
XM_017009963.2:c.664G>A XP_016865452.1:p.Asp222Asn
XM_017009964.2:c.664G>A XP_016865453.1:p.Asp222Asn
XM_017009965.1:c.661G>A XP_016865454.1:p.Asp221Asn
XM_017009966.2:c.664G>A XP_016865455.1:p.Asp222Asn
XM_017009967.1:c.568G>A XP_016865456.1:p.Asp190Asn
XM_017009968.2:c.664G>A XP_016865457.1:p.Asp222Asn
XM_017009969.2:c.664G>A XP_016865458.1:p.Asp222Asn
XM_017009970.2:c.664G>A XP_016865459.1:p.Asp222Asn
XM_017009971.2:c.664G>A XP_016865460.1:p.Asp222Asn
XM_017009974.2:c.664G>A XP_016865463.1:p.Asp222Asn