Canonical Allele Identifier: CA360397515

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012457A>G (hg19) ; chr5:g.90716640A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716640A>G , CM000667.2:g.90716640A>G	GRCh38
NC_000005.9:g.90012457A>G , CM000667.1:g.90012457A>G	GRCh37
NC_000005.8:g.90048213A>G	NCBI36
NG_007083.1:g.162841A>G
NG_007083.2:g.192297A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9358A>G MANE Select	ENSP00000384582.2:p.Ile3120Val
ENST00000639431.1:c.265+40431A>G	ENSP00000491057.1:n.265+40431A>G
ENST00000639473.1:n.4817A>G
ENST00000640012.1:c.3165A>G
ENST00000640374.1:n.2502A>G
ENST00000640779.1:c.4087A>G
ENST00000405460.6:c.9358A>G	ENSP00000384582.2:p.Ile3120Val
ENST00000509621.1:c.2055A>G
NM_032119.3:c.9358A>G	NP_115495.3:p.Ile3120Val
NR_003149.1:n.9371A>G
XM_011543675.1:c.9355A>G	XP_011541977.1:p.Ile3119Val
XM_011543676.1:c.9277A>G	XP_011541978.1:p.Ile3093Val
XM_011543677.1:c.6661A>G	XP_011541979.1:p.Ile2221Val
XM_011543678.1:c.9358A>G	XP_011541980.1:p.Ile3120Val
XM_011543679.1:c.9358A>G	XP_011541981.1:p.Ile3120Val
XR_948560.1:n.272-831T>C
NM_032119.4:c.9358A>G MANE Select	NP_115495.3:p.Ile3120Val
XM_017009963.2:c.9379A>G	XP_016865452.1:p.Ile3127Val
XM_017009964.2:c.9376A>G	XP_016865453.1:p.Ile3126Val
XM_017009965.1:c.9376A>G	XP_016865454.1:p.Ile3126Val
XM_017009966.2:c.9298A>G	XP_016865455.1:p.Ile3100Val
XM_017009967.1:c.9283A>G	XP_016865456.1:p.Ile3095Val
XM_017009968.2:c.9379A>G	XP_016865457.1:p.Ile3127Val
XM_017009969.2:c.9379A>G	XP_016865458.1:p.Ile3127Val
XM_017009970.2:c.9379A>G	XP_016865459.1:p.Ile3127Val
XM_017009971.2:c.9379A>G	XP_016865460.1:p.Ile3127Val
XM_017009972.1:c.2497A>G	XP_016865461.1:p.Ile833Val
XM_017009973.1:c.2476A>G	XP_016865462.1:p.Ile826Val
XM_017009974.2:c.9379A>G	XP_016865463.1:p.Ile3127Val
XR_001742802.1:n.2523-831T>C
NR_003149.2:n.9374A>G