Canonical Allele Identifier: CA360366728

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90050892C>G (hg19) ; chr5:g.90755075C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90755075C>G , CM000667.2:g.90755075C>G	GRCh38
NC_000005.9:g.90050892C>G , CM000667.1:g.90050892C>G	GRCh37
NC_000005.8:g.90086648C>G	NCBI36
NG_007083.1:g.201276C>G
NG_007083.2:g.230732C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.11470C>G MANE Select	ENSP00000384582.2:p.Leu3824Val
ENST00000425867.3:c.601C>G	ENSP00000392618.3:p.Leu201Val
ENST00000639431.1:c.265+78866C>G	ENSP00000491057.1:n.265+78866C>G
ENST00000640374.1:n.4614C>G
ENST00000640464.1:n.1889C>G
ENST00000405460.6:c.11470C>G	ENSP00000384582.2:p.Leu3824Val
ENST00000509621.1:c.4167C>G
NM_032119.3:c.11470C>G	NP_115495.3:p.Leu3824Val
NR_003149.1:n.11483C>G
XM_011543675.1:c.11467C>G	XP_011541977.1:p.Leu3823Val
XM_011543676.1:c.11389C>G	XP_011541978.1:p.Leu3797Val
XM_011543677.1:c.8773C>G	XP_011541979.1:p.Leu2925Val
XM_011543678.1:c.11470C>G	XP_011541980.1:p.Leu3824Val
NM_032119.4:c.11470C>G MANE Select	NP_115495.3:p.Leu3824Val
XM_017009963.2:c.11491C>G	XP_016865452.1:p.Leu3831Val
XM_017009964.2:c.11488C>G	XP_016865453.1:p.Leu3830Val
XM_017009965.1:c.11488C>G	XP_016865454.1:p.Leu3830Val
XM_017009966.2:c.11410C>G	XP_016865455.1:p.Leu3804Val
XM_017009967.1:c.11395C>G	XP_016865456.1:p.Leu3799Val
XM_017009968.2:c.11491C>G	XP_016865457.1:p.Leu3831Val
XM_017009969.2:c.11491C>G	XP_016865458.1:p.Leu3831Val
XM_017009970.2:c.11491C>G	XP_016865459.1:p.Leu3831Val
XM_017009971.2:c.11491C>G	XP_016865460.1:p.Leu3831Val
XM_017009972.1:c.4609C>G	XP_016865461.1:p.Leu1537Val
XM_017009973.1:c.4588C>G	XP_016865462.1:p.Leu1530Val
NR_003149.2:n.11486C>G