Canonical Allele Identifier: CA360397661

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012496C>G (hg19) ; chr5:g.90716679C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716679C>G , CM000667.2:g.90716679C>G	GRCh38
NC_000005.9:g.90012496C>G , CM000667.1:g.90012496C>G	GRCh37
NC_000005.8:g.90048252C>G	NCBI36
NG_007083.1:g.162880C>G
NG_007083.2:g.192336C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9397C>G MANE Select	ENSP00000384582.2:p.Leu3133Val
ENST00000639431.1:c.265+40470C>G	ENSP00000491057.1:n.265+40470C>G
ENST00000639473.1:n.4856C>G
ENST00000640012.1:c.3204C>G
ENST00000640374.1:n.2541C>G
ENST00000640779.1:c.4126C>G
ENST00000405460.6:c.9397C>G	ENSP00000384582.2:p.Leu3133Val
ENST00000509621.1:c.2094C>G
NM_032119.3:c.9397C>G	NP_115495.3:p.Leu3133Val
NR_003149.1:n.9410C>G
XM_011543675.1:c.9394C>G	XP_011541977.1:p.Leu3132Val
XM_011543676.1:c.9316C>G	XP_011541978.1:p.Leu3106Val
XM_011543677.1:c.6700C>G	XP_011541979.1:p.Leu2234Val
XM_011543678.1:c.9397C>G	XP_011541980.1:p.Leu3133Val
XM_011543679.1:c.9397C>G	XP_011541981.1:p.Leu3133Val
XR_948560.1:n.272-870G>C
NM_032119.4:c.9397C>G MANE Select	NP_115495.3:p.Leu3133Val
XM_017009963.2:c.9418C>G	XP_016865452.1:p.Leu3140Val
XM_017009964.2:c.9415C>G	XP_016865453.1:p.Leu3139Val
XM_017009965.1:c.9415C>G	XP_016865454.1:p.Leu3139Val
XM_017009966.2:c.9337C>G	XP_016865455.1:p.Leu3113Val
XM_017009967.1:c.9322C>G	XP_016865456.1:p.Leu3108Val
XM_017009968.2:c.9418C>G	XP_016865457.1:p.Leu3140Val
XM_017009969.2:c.9418C>G	XP_016865458.1:p.Leu3140Val
XM_017009970.2:c.9418C>G	XP_016865459.1:p.Leu3140Val
XM_017009971.2:c.9418C>G	XP_016865460.1:p.Leu3140Val
XM_017009972.1:c.2536C>G	XP_016865461.1:p.Leu846Val
XM_017009973.1:c.2515C>G	XP_016865462.1:p.Leu839Val
XM_017009974.2:c.9418C>G	XP_016865463.1:p.Leu3140Val
XR_001742802.1:n.2523-870G>C
NR_003149.2:n.9413C>G