Canonical Allele Identifier: CA445404048

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050861C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755044C>T , CM000667.2:g.90755044C>T	GRCh38
NC_000005.9:g.90050861C>T , CM000667.1:g.90050861C>T	GRCh37
NC_000005.8:g.90086617C>T	NCBI36
NG_007083.1:g.201245C>T
NG_007083.2:g.230701C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11439C>T MANE Select	ENSP00000384582.2:p.Ala3813=
ENST00000425867.3:c.570C>T	ENSP00000392618.3:p.Ala190=
ENST00000639431.1:c.265+78835C>T	ENSP00000491057.1:n.265+78835C>T
ENST00000640374.1:n.4583C>T
ENST00000640464.1:n.1858C>T
ENST00000405460.6:c.11439C>T	ENSP00000384582.2:p.Ala3813=
ENST00000509621.1:c.4136C>T
NM_032119.3:c.11439C>T	NP_115495.3:p.Ala3813=
NR_003149.1:n.11452C>T
XM_011543675.1:c.11436C>T	XP_011541977.1:p.Ala3812=
XM_011543676.1:c.11358C>T	XP_011541978.1:p.Ala3786=
XM_011543677.1:c.8742C>T	XP_011541979.1:p.Ala2914=
XM_011543678.1:c.11439C>T	XP_011541980.1:p.Ala3813=
NM_032119.4:c.11439C>T MANE Select	NP_115495.3:p.Ala3813=
XM_017009963.2:c.11460C>T	XP_016865452.1:p.Ala3820=
XM_017009964.2:c.11457C>T	XP_016865453.1:p.Ala3819=
XM_017009965.1:c.11457C>T	XP_016865454.1:p.Ala3819=
XM_017009966.2:c.11379C>T	XP_016865455.1:p.Ala3793=
XM_017009967.1:c.11364C>T	XP_016865456.1:p.Ala3788=
XM_017009968.2:c.11460C>T	XP_016865457.1:p.Ala3820=
XM_017009969.2:c.11460C>T	XP_016865458.1:p.Ala3820=
XM_017009970.2:c.11460C>T	XP_016865459.1:p.Ala3820=
XM_017009971.2:c.11460C>T	XP_016865460.1:p.Ala3820=
XM_017009972.1:c.4578C>T	XP_016865461.1:p.Ala1526=
XM_017009973.1:c.4557C>T	XP_016865462.1:p.Ala1519=
NR_003149.2:n.11455C>T