Canonical Allele Identifier: CA445416061

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041456A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745639A>T , CM000667.2:g.90745639A>T	GRCh38
NC_000005.9:g.90041456A>T , CM000667.1:g.90041456A>T	GRCh37
NC_000005.8:g.90077212A>T	NCBI36
NG_007083.1:g.191840A>T
NG_007083.2:g.221296A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10818A>T MANE Select	ENSP00000384582.2:p.Ala3606=
ENST00000639431.1:c.265+69430A>T	ENSP00000491057.1:n.265+69430A>T
ENST00000640374.1:n.3962A>T
ENST00000640464.1:n.1237A>T
ENST00000405460.6:c.10818A>T	ENSP00000384582.2:p.Ala3606=
ENST00000509621.1:c.3515A>T
NM_032119.3:c.10818A>T	NP_115495.3:p.Ala3606=
NR_003149.1:n.10831A>T
XM_011543675.1:c.10815A>T	XP_011541977.1:p.Ala3605=
XM_011543676.1:c.10737A>T	XP_011541978.1:p.Ala3579=
XM_011543677.1:c.8121A>T	XP_011541979.1:p.Ala2707=
XM_011543678.1:c.10818A>T	XP_011541980.1:p.Ala3606=
XM_011543679.1:c.*40A>T	XP_011541981.1:n.*40A>T
NM_032119.4:c.10818A>T MANE Select	NP_115495.3:p.Ala3606=
XM_017009963.2:c.10839A>T	XP_016865452.1:p.Ala3613=
XM_017009964.2:c.10836A>T	XP_016865453.1:p.Ala3612=
XM_017009965.1:c.10836A>T	XP_016865454.1:p.Ala3612=
XM_017009966.2:c.10758A>T	XP_016865455.1:p.Ala3586=
XM_017009967.1:c.10743A>T	XP_016865456.1:p.Ala3581=
XM_017009968.2:c.10839A>T	XP_016865457.1:p.Ala3613=
XM_017009969.2:c.10839A>T	XP_016865458.1:p.Ala3613=
XM_017009970.2:c.10839A>T	XP_016865459.1:p.Ala3613=
XM_017009971.2:c.10839A>T	XP_016865460.1:p.Ala3613=
XM_017009972.1:c.3957A>T	XP_016865461.1:p.Ala1319=
XM_017009973.1:c.3936A>T	XP_016865462.1:p.Ala1312=
XM_017009974.2:c.*40A>T	XP_016865463.1:n.*40A>T
NR_003149.2:n.10834A>T