Canonical Allele Identifier: CA360366442

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050847C>G (hg19) ; chr5:g.90755030C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755030C>G , CM000667.2:g.90755030C>G	GRCh38
NC_000005.9:g.90050847C>G , CM000667.1:g.90050847C>G	GRCh37
NC_000005.8:g.90086603C>G	NCBI36
NG_007083.1:g.201231C>G
NG_007083.2:g.230687C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.11425C>G MANE Select	ENSP00000384582.2:p.Leu3809Val
ENST00000425867.3:c.556C>G	ENSP00000392618.3:p.Leu186Val
ENST00000639431.1:c.265+78821C>G	ENSP00000491057.1:n.265+78821C>G
ENST00000640374.1:n.4569C>G
ENST00000640464.1:n.1844C>G
ENST00000405460.6:c.11425C>G	ENSP00000384582.2:p.Leu3809Val
ENST00000509621.1:c.4122C>G
NM_032119.3:c.11425C>G	NP_115495.3:p.Leu3809Val
NR_003149.1:n.11438C>G
XM_011543675.1:c.11422C>G	XP_011541977.1:p.Leu3808Val
XM_011543676.1:c.11344C>G	XP_011541978.1:p.Leu3782Val
XM_011543677.1:c.8728C>G	XP_011541979.1:p.Leu2910Val
XM_011543678.1:c.11425C>G	XP_011541980.1:p.Leu3809Val
NM_032119.4:c.11425C>G MANE Select	NP_115495.3:p.Leu3809Val
XM_017009963.2:c.11446C>G	XP_016865452.1:p.Leu3816Val
XM_017009964.2:c.11443C>G	XP_016865453.1:p.Leu3815Val
XM_017009965.1:c.11443C>G	XP_016865454.1:p.Leu3815Val
XM_017009966.2:c.11365C>G	XP_016865455.1:p.Leu3789Val
XM_017009967.1:c.11350C>G	XP_016865456.1:p.Leu3784Val
XM_017009968.2:c.11446C>G	XP_016865457.1:p.Leu3816Val
XM_017009969.2:c.11446C>G	XP_016865458.1:p.Leu3816Val
XM_017009970.2:c.11446C>G	XP_016865459.1:p.Leu3816Val
XM_017009971.2:c.11446C>G	XP_016865460.1:p.Leu3816Val
XM_017009972.1:c.4564C>G	XP_016865461.1:p.Leu1522Val
XM_017009973.1:c.4543C>G	XP_016865462.1:p.Leu1515Val
NR_003149.2:n.11441C>G