Canonical Allele Identifier: CA445404528

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988529C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692712C>T , CM000667.2:g.90692712C>T	GRCh38
NC_000005.9:g.89988529C>T , CM000667.1:g.89988529C>T	GRCh37
NC_000005.8:g.90024285C>T	NCBI36
NG_007083.1:g.138913C>T
NG_007083.2:g.168369C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7059C>T MANE Select	ENSP00000384582.2:p.Ala2353=
ENST00000639431.1:c.265+16503C>T	ENSP00000491057.1:n.265+16503C>T
ENST00000639473.1:n.2518C>T
ENST00000640012.1:c.866C>T
ENST00000640374.1:n.203C>T
ENST00000640403.1:c.4350C>T	ENSP00000492531.1:p.Ala1450=
ENST00000640779.1:c.1788C>T
ENST00000405460.6:c.7059C>T	ENSP00000384582.2:p.Ala2353=
NM_032119.3:c.7059C>T	NP_115495.3:p.Ala2353=
NR_003149.1:n.7072C>T
XM_011543675.1:c.7056C>T	XP_011541977.1:p.Ala2352=
XM_011543676.1:c.6978C>T	XP_011541978.1:p.Ala2326=
XM_011543677.1:c.4362C>T	XP_011541979.1:p.Ala1454=
XM_011543678.1:c.7059C>T	XP_011541980.1:p.Ala2353=
XM_011543679.1:c.7059C>T	XP_011541981.1:p.Ala2353=
NM_032119.4:c.7059C>T MANE Select	NP_115495.3:p.Ala2353=
XM_017009963.2:c.7059C>T	XP_016865452.1:p.Ala2353=
XM_017009964.2:c.7056C>T	XP_016865453.1:p.Ala2352=
XM_017009965.1:c.7056C>T	XP_016865454.1:p.Ala2352=
XM_017009966.2:c.6978C>T	XP_016865455.1:p.Ala2326=
XM_017009967.1:c.6963C>T	XP_016865456.1:p.Ala2321=
XM_017009968.2:c.7059C>T	XP_016865457.1:p.Ala2353=
XM_017009969.2:c.7059C>T	XP_016865458.1:p.Ala2353=
XM_017009970.2:c.7059C>T	XP_016865459.1:p.Ala2353=
XM_017009971.2:c.7059C>T	XP_016865460.1:p.Ala2353=
XM_017009972.1:c.177C>T	XP_016865461.1:p.Ala59=
XM_017009973.1:c.177C>T	XP_016865462.1:p.Ala59=
XM_017009974.2:c.7059C>T	XP_016865463.1:p.Ala2353=
NR_003149.2:n.7075C>T