Canonical Allele Identifier: CA360388613

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89999488T>G (hg19) ; chr5:g.90703671T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90703671T>G , CM000667.2:g.90703671T>G	GRCh38
NC_000005.9:g.89999488T>G , CM000667.1:g.89999488T>G	GRCh37
NC_000005.8:g.90035244T>G	NCBI36
NG_007083.1:g.149872T>G
NG_007083.2:g.179328T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.8162T>G MANE Select	ENSP00000384582.2:p.Ile2721Ser
ENST00000639431.1:c.265+27462T>G	ENSP00000491057.1:n.265+27462T>G
ENST00000639473.1:n.3621T>G
ENST00000640012.1:c.1969T>G
ENST00000640374.1:n.1306T>G
ENST00000640403.1:c.5453T>G	ENSP00000492531.1:p.Ile1818Ser
ENST00000640779.1:c.2891T>G
ENST00000405460.6:c.8162T>G	ENSP00000384582.2:p.Ile2721Ser
ENST00000509621.1:c.859T>G
NM_032119.3:c.8162T>G	NP_115495.3:p.Ile2721Ser
NR_003149.1:n.8175T>G
XM_011543675.1:c.8159T>G	XP_011541977.1:p.Ile2720Ser
XM_011543676.1:c.8081T>G	XP_011541978.1:p.Ile2694Ser
XM_011543677.1:c.5465T>G	XP_011541979.1:p.Ile1822Ser
XM_011543678.1:c.8162T>G	XP_011541980.1:p.Ile2721Ser
XM_011543679.1:c.8162T>G	XP_011541981.1:p.Ile2721Ser
NM_032119.4:c.8162T>G MANE Select	NP_115495.3:p.Ile2721Ser
XM_017009963.2:c.8162T>G	XP_016865452.1:p.Ile2721Ser
XM_017009964.2:c.8159T>G	XP_016865453.1:p.Ile2720Ser
XM_017009965.1:c.8159T>G	XP_016865454.1:p.Ile2720Ser
XM_017009966.2:c.8081T>G	XP_016865455.1:p.Ile2694Ser
XM_017009967.1:c.8066T>G	XP_016865456.1:p.Ile2689Ser
XM_017009968.2:c.8162T>G	XP_016865457.1:p.Ile2721Ser
XM_017009969.2:c.8162T>G	XP_016865458.1:p.Ile2721Ser
XM_017009970.2:c.8162T>G	XP_016865459.1:p.Ile2721Ser
XM_017009971.2:c.8162T>G	XP_016865460.1:p.Ile2721Ser
XM_017009972.1:c.1280T>G	XP_016865461.1:p.Ile427Ser
XM_017009973.1:c.1280T>G	XP_016865462.1:p.Ile427Ser
XM_017009974.2:c.8162T>G	XP_016865463.1:p.Ile2721Ser
NR_003149.2:n.8178T>G