Canonical Allele Identifier: CA445436398

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90119251A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90823434A>G , CM000667.2:g.90823434A>G	GRCh38
NC_000005.9:g.90119251A>G , CM000667.1:g.90119251A>G	GRCh37
NC_000005.8:g.90155007A>G	NCBI36
NG_007083.1:g.269635A>G
NG_007083.2:g.299091A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.16206A>G MANE Select	ENSP00000384582.2:p.Glu5402=
ENST00000425867.3:c.5160A>G	ENSP00000392618.3:p.Glu1720=
ENST00000638510.1:n.3473A>G
ENST00000639431.1:c.265+147225A>G	ENSP00000491057.1:n.265+147225A>G
ENST00000640061.1:n.128+1252A>G
ENST00000640407.1:c.2616A>G	ENSP00000491425.1:p.Glu872=
ENST00000405460.6:c.16206A>G	ENSP00000384582.2:p.Glu5402=
ENST00000425867.2:c.3189A>G	ENSP00000392618.2:p.Glu1063=
NM_032119.3:c.16206A>G	NP_115495.3:p.Glu5402=
NR_003149.1:n.16219A>G
XM_011543675.1:c.16203A>G	XP_011541977.1:p.Glu5401=
XM_011543676.1:c.16125A>G	XP_011541978.1:p.Glu5375=
XM_011543677.1:c.13509A>G	XP_011541979.1:p.Glu4503=
NM_032119.4:c.16206A>G MANE Select	NP_115495.3:p.Glu5402=
XM_017009963.2:c.16227A>G	XP_016865452.1:p.Glu5409=
XM_017009964.2:c.16224A>G	XP_016865453.1:p.Glu5408=
XM_017009965.1:c.16224A>G	XP_016865454.1:p.Glu5408=
XM_017009966.2:c.16146A>G	XP_016865455.1:p.Glu5382=
XM_017009967.1:c.16131A>G	XP_016865456.1:p.Glu5377=
XM_017009968.2:c.16047A>G	XP_016865457.1:p.Glu5349=
XM_017009969.2:c.16227A>G	XP_016865458.1:p.Glu5409=
XM_017009972.1:c.9345A>G	XP_016865461.1:p.Glu3115=
XM_017009973.1:c.9324A>G	XP_016865462.1:p.Glu3108=
NR_003149.2:n.16222A>G