Canonical Allele Identifier: CA360366433

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050844C>G (hg19) ; chr5:g.90755027C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755027C>G , CM000667.2:g.90755027C>G	GRCh38
NC_000005.9:g.90050844C>G , CM000667.1:g.90050844C>G	GRCh37
NC_000005.8:g.90086600C>G	NCBI36
NG_007083.1:g.201228C>G
NG_007083.2:g.230684C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11422C>G MANE Select	ENSP00000384582.2:p.Leu3808Val
ENST00000425867.3:c.553C>G	ENSP00000392618.3:p.Leu185Val
ENST00000639431.1:c.265+78818C>G	ENSP00000491057.1:n.265+78818C>G
ENST00000640374.1:n.4566C>G
ENST00000640464.1:n.1841C>G
ENST00000405460.6:c.11422C>G	ENSP00000384582.2:p.Leu3808Val
ENST00000509621.1:c.4119C>G
NM_032119.3:c.11422C>G	NP_115495.3:p.Leu3808Val
NR_003149.1:n.11435C>G
XM_011543675.1:c.11419C>G	XP_011541977.1:p.Leu3807Val
XM_011543676.1:c.11341C>G	XP_011541978.1:p.Leu3781Val
XM_011543677.1:c.8725C>G	XP_011541979.1:p.Leu2909Val
XM_011543678.1:c.11422C>G	XP_011541980.1:p.Leu3808Val
NM_032119.4:c.11422C>G MANE Select	NP_115495.3:p.Leu3808Val
XM_017009963.2:c.11443C>G	XP_016865452.1:p.Leu3815Val
XM_017009964.2:c.11440C>G	XP_016865453.1:p.Leu3814Val
XM_017009965.1:c.11440C>G	XP_016865454.1:p.Leu3814Val
XM_017009966.2:c.11362C>G	XP_016865455.1:p.Leu3788Val
XM_017009967.1:c.11347C>G	XP_016865456.1:p.Leu3783Val
XM_017009968.2:c.11443C>G	XP_016865457.1:p.Leu3815Val
XM_017009969.2:c.11443C>G	XP_016865458.1:p.Leu3815Val
XM_017009970.2:c.11443C>G	XP_016865459.1:p.Leu3815Val
XM_017009971.2:c.11443C>G	XP_016865460.1:p.Leu3815Val
XM_017009972.1:c.4561C>G	XP_016865461.1:p.Leu1521Val
XM_017009973.1:c.4540C>G	XP_016865462.1:p.Leu1514Val
NR_003149.2:n.11438C>G