Canonical Allele Identifier: CA445414033

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012531A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716714A>G , CM000667.2:g.90716714A>G	GRCh38
NC_000005.9:g.90012531A>G , CM000667.1:g.90012531A>G	GRCh37
NC_000005.8:g.90048287A>G	NCBI36
NG_007083.1:g.162915A>G
NG_007083.2:g.192371A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9432A>G MANE Select	ENSP00000384582.2:p.Glu3144=
ENST00000639431.1:c.265+40505A>G	ENSP00000491057.1:n.265+40505A>G
ENST00000639473.1:n.4891A>G
ENST00000640012.1:c.3239A>G
ENST00000640374.1:n.2576A>G
ENST00000640779.1:c.4161A>G
ENST00000405460.6:c.9432A>G	ENSP00000384582.2:p.Glu3144=
ENST00000509621.1:c.2129A>G
NM_032119.3:c.9432A>G	NP_115495.3:p.Glu3144=
NR_003149.1:n.9445A>G
XM_011543675.1:c.9429A>G	XP_011541977.1:p.Glu3143=
XM_011543676.1:c.9351A>G	XP_011541978.1:p.Glu3117=
XM_011543677.1:c.6735A>G	XP_011541979.1:p.Glu2245=
XM_011543678.1:c.9432A>G	XP_011541980.1:p.Glu3144=
XM_011543679.1:c.9432A>G	XP_011541981.1:p.Glu3144=
XR_948560.1:n.272-905T>C
NM_032119.4:c.9432A>G MANE Select	NP_115495.3:p.Glu3144=
XM_017009963.2:c.9453A>G	XP_016865452.1:p.Glu3151=
XM_017009964.2:c.9450A>G	XP_016865453.1:p.Glu3150=
XM_017009965.1:c.9450A>G	XP_016865454.1:p.Glu3150=
XM_017009966.2:c.9372A>G	XP_016865455.1:p.Glu3124=
XM_017009967.1:c.9357A>G	XP_016865456.1:p.Glu3119=
XM_017009968.2:c.9453A>G	XP_016865457.1:p.Glu3151=
XM_017009969.2:c.9453A>G	XP_016865458.1:p.Glu3151=
XM_017009970.2:c.9453A>G	XP_016865459.1:p.Glu3151=
XM_017009971.2:c.9453A>G	XP_016865460.1:p.Glu3151=
XM_017009972.1:c.2571A>G	XP_016865461.1:p.Glu857=
XM_017009973.1:c.2550A>G	XP_016865462.1:p.Glu850=
XM_017009974.2:c.9453A>G	XP_016865463.1:p.Glu3151=
XR_001742802.1:n.2523-905T>C
NR_003149.2:n.9448A>G