Canonical Allele Identifier: CA360366740

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050895C>A (hg19) ; chr5:g.90755078C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755078C>A , CM000667.2:g.90755078C>A	GRCh38
NC_000005.9:g.90050895C>A , CM000667.1:g.90050895C>A	GRCh37
NC_000005.8:g.90086651C>A	NCBI36
NG_007083.1:g.201279C>A
NG_007083.2:g.230735C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11473C>A MANE Select	ENSP00000384582.2:p.His3825Asn
ENST00000425867.3:c.604C>A	ENSP00000392618.3:p.His202Asn
ENST00000639431.1:c.265+78869C>A	ENSP00000491057.1:n.265+78869C>A
ENST00000640374.1:n.4617C>A
ENST00000640464.1:n.1892C>A
ENST00000405460.6:c.11473C>A	ENSP00000384582.2:p.His3825Asn
ENST00000509621.1:c.4170C>A
NM_032119.3:c.11473C>A	NP_115495.3:p.His3825Asn
NR_003149.1:n.11486C>A
XM_011543675.1:c.11470C>A	XP_011541977.1:p.His3824Asn
XM_011543676.1:c.11392C>A	XP_011541978.1:p.His3798Asn
XM_011543677.1:c.8776C>A	XP_011541979.1:p.His2926Asn
XM_011543678.1:c.11473C>A	XP_011541980.1:p.His3825Asn
NM_032119.4:c.11473C>A MANE Select	NP_115495.3:p.His3825Asn
XM_017009963.2:c.11494C>A	XP_016865452.1:p.His3832Asn
XM_017009964.2:c.11491C>A	XP_016865453.1:p.His3831Asn
XM_017009965.1:c.11491C>A	XP_016865454.1:p.His3831Asn
XM_017009966.2:c.11413C>A	XP_016865455.1:p.His3805Asn
XM_017009967.1:c.11398C>A	XP_016865456.1:p.His3800Asn
XM_017009968.2:c.11494C>A	XP_016865457.1:p.His3832Asn
XM_017009969.2:c.11494C>A	XP_016865458.1:p.His3832Asn
XM_017009970.2:c.11494C>A	XP_016865459.1:p.His3832Asn
XM_017009971.2:c.11494C>A	XP_016865460.1:p.His3832Asn
XM_017009972.1:c.4612C>A	XP_016865461.1:p.His1538Asn
XM_017009973.1:c.4591C>A	XP_016865462.1:p.His1531Asn
NR_003149.2:n.11489C>A