Canonical Allele Identifier: CA360397672

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012500C>G (hg19) ; chr5:g.90716683C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716683C>G , CM000667.2:g.90716683C>G	GRCh38
NC_000005.9:g.90012500C>G , CM000667.1:g.90012500C>G	GRCh37
NC_000005.8:g.90048256C>G	NCBI36
NG_007083.1:g.162884C>G
NG_007083.2:g.192340C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9401C>G MANE Select	ENSP00000384582.2:p.Thr3134Ser
ENST00000639431.1:c.265+40474C>G	ENSP00000491057.1:n.265+40474C>G
ENST00000639473.1:n.4860C>G
ENST00000640012.1:c.3208C>G
ENST00000640374.1:n.2545C>G
ENST00000640779.1:c.4130C>G
ENST00000405460.6:c.9401C>G	ENSP00000384582.2:p.Thr3134Ser
ENST00000509621.1:c.2098C>G
NM_032119.3:c.9401C>G	NP_115495.3:p.Thr3134Ser
NR_003149.1:n.9414C>G
XM_011543675.1:c.9398C>G	XP_011541977.1:p.Thr3133Ser
XM_011543676.1:c.9320C>G	XP_011541978.1:p.Thr3107Ser
XM_011543677.1:c.6704C>G	XP_011541979.1:p.Thr2235Ser
XM_011543678.1:c.9401C>G	XP_011541980.1:p.Thr3134Ser
XM_011543679.1:c.9401C>G	XP_011541981.1:p.Thr3134Ser
XR_948560.1:n.272-874G>C
NM_032119.4:c.9401C>G MANE Select	NP_115495.3:p.Thr3134Ser
XM_017009963.2:c.9422C>G	XP_016865452.1:p.Thr3141Ser
XM_017009964.2:c.9419C>G	XP_016865453.1:p.Thr3140Ser
XM_017009965.1:c.9419C>G	XP_016865454.1:p.Thr3140Ser
XM_017009966.2:c.9341C>G	XP_016865455.1:p.Thr3114Ser
XM_017009967.1:c.9326C>G	XP_016865456.1:p.Thr3109Ser
XM_017009968.2:c.9422C>G	XP_016865457.1:p.Thr3141Ser
XM_017009969.2:c.9422C>G	XP_016865458.1:p.Thr3141Ser
XM_017009970.2:c.9422C>G	XP_016865459.1:p.Thr3141Ser
XM_017009971.2:c.9422C>G	XP_016865460.1:p.Thr3141Ser
XM_017009972.1:c.2540C>G	XP_016865461.1:p.Thr847Ser
XM_017009973.1:c.2519C>G	XP_016865462.1:p.Thr840Ser
XM_017009974.2:c.9422C>G	XP_016865463.1:p.Thr3141Ser
XR_001742802.1:n.2523-874G>C
NR_003149.2:n.9417C>G