Canonical Allele Identifier: CA360414036

Gene: ADGRV1

Linked Data

• COSMIC: COSM3920464
• MyVariant Identifiers: chr5:g.89979796G>A (hg19) ; chr5:g.90683979G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90683979G>A , CM000667.2:g.90683979G>A	GRCh38
NC_000005.9:g.89979796G>A , CM000667.1:g.89979796G>A	GRCh37
NC_000005.8:g.90015552G>A	NCBI36
NG_007083.1:g.130180G>A
NG_007083.2:g.159636G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6058G>A MANE Select	ENSP00000384582.2:p.Asp2020Asn
ENST00000639431.1:c.265+7770G>A	ENSP00000491057.1:n.265+7770G>A
ENST00000639473.1:n.1517G>A
ENST00000640012.1:c.165-1801G>A
ENST00000640403.1:c.3349G>A	ENSP00000492531.1:p.Asp1117Asn
ENST00000640779.1:c.870G>A
ENST00000405460.6:c.6058G>A	ENSP00000384582.2:p.Asp2020Asn
NM_032119.3:c.6058G>A	NP_115495.3:p.Asp2020Asn
NR_003149.1:n.6154G>A
XM_011543675.1:c.6055G>A	XP_011541977.1:p.Asp2019Asn
XM_011543676.1:c.5977G>A	XP_011541978.1:p.Asp1993Asn
XM_011543677.1:c.3361G>A	XP_011541979.1:p.Asp1121Asn
XM_011543678.1:c.6058G>A	XP_011541980.1:p.Asp2020Asn
XM_011543679.1:c.6058G>A	XP_011541981.1:p.Asp2020Asn
NM_032119.4:c.6058G>A MANE Select	NP_115495.3:p.Asp2020Asn
XM_017009963.2:c.6058G>A	XP_016865452.1:p.Asp2020Asn
XM_017009964.2:c.6055G>A	XP_016865453.1:p.Asp2019Asn
XM_017009965.1:c.6055G>A	XP_016865454.1:p.Asp2019Asn
XM_017009966.2:c.5977G>A	XP_016865455.1:p.Asp1993Asn
XM_017009967.1:c.5962G>A	XP_016865456.1:p.Asp1988Asn
XM_017009968.2:c.6058G>A	XP_016865457.1:p.Asp2020Asn
XM_017009969.2:c.6058G>A	XP_016865458.1:p.Asp2020Asn
XM_017009970.2:c.6058G>A	XP_016865459.1:p.Asp2020Asn
XM_017009971.2:c.6058G>A	XP_016865460.1:p.Asp2020Asn
XM_017009973.1:c.-742G>A	XP_016865462.1:n.-742G>A
XM_017009974.2:c.6058G>A	XP_016865463.1:p.Asp2020Asn
NR_003149.2:n.6157G>A