Canonical Allele Identifier: CA360366950

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050925G>A (hg19) ; chr5:g.90755108G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755108G>A , CM000667.2:g.90755108G>A	GRCh38
NC_000005.9:g.90050925G>A , CM000667.1:g.90050925G>A	GRCh37
NC_000005.8:g.90086681G>A	NCBI36
NG_007083.1:g.201309G>A
NG_007083.2:g.230765G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11503G>A MANE Select	ENSP00000384582.2:p.Asp3835Asn
ENST00000425867.3:c.634G>A	ENSP00000392618.3:p.Asp212Asn
ENST00000639431.1:c.265+78899G>A	ENSP00000491057.1:n.265+78899G>A
ENST00000640374.1:n.4647G>A
ENST00000640464.1:n.1922G>A
ENST00000405460.6:c.11503G>A	ENSP00000384582.2:p.Asp3835Asn
ENST00000509621.1:c.4200G>A
NM_032119.3:c.11503G>A	NP_115495.3:p.Asp3835Asn
NR_003149.1:n.11516G>A
XM_011543675.1:c.11500G>A	XP_011541977.1:p.Asp3834Asn
XM_011543676.1:c.11422G>A	XP_011541978.1:p.Asp3808Asn
XM_011543677.1:c.8806G>A	XP_011541979.1:p.Asp2936Asn
XM_011543678.1:c.11503G>A	XP_011541980.1:p.Asp3835Asn
NM_032119.4:c.11503G>A MANE Select	NP_115495.3:p.Asp3835Asn
XM_017009963.2:c.11524G>A	XP_016865452.1:p.Asp3842Asn
XM_017009964.2:c.11521G>A	XP_016865453.1:p.Asp3841Asn
XM_017009965.1:c.11521G>A	XP_016865454.1:p.Asp3841Asn
XM_017009966.2:c.11443G>A	XP_016865455.1:p.Asp3815Asn
XM_017009967.1:c.11428G>A	XP_016865456.1:p.Asp3810Asn
XM_017009968.2:c.11524G>A	XP_016865457.1:p.Asp3842Asn
XM_017009969.2:c.11524G>A	XP_016865458.1:p.Asp3842Asn
XM_017009970.2:c.11524G>A	XP_016865459.1:p.Asp3842Asn
XM_017009971.2:c.11524G>A	XP_016865460.1:p.Asp3842Asn
XM_017009972.1:c.4642G>A	XP_016865461.1:p.Asp1548Asn
XM_017009973.1:c.4621G>A	XP_016865462.1:p.Asp1541Asn
NR_003149.2:n.11519G>A