Canonical Allele Identifier: CA360396172

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008131T>G (hg19) ; chr5:g.90712314T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712314T>G , CM000667.2:g.90712314T>G	GRCh38
NC_000005.9:g.90008131T>G , CM000667.1:g.90008131T>G	GRCh37
NC_000005.8:g.90043887T>G	NCBI36
NG_007083.1:g.158515T>G
NG_007083.2:g.187971T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9070T>G MANE Select	ENSP00000384582.2:p.Tyr3024Asp
ENST00000639431.1:c.265+36105T>G	ENSP00000491057.1:n.265+36105T>G
ENST00000639473.1:n.4529T>G
ENST00000640012.1:c.2877T>G
ENST00000640374.1:n.2214T>G
ENST00000640779.1:c.3799T>G
ENST00000405460.6:c.9070T>G	ENSP00000384582.2:p.Tyr3024Asp
ENST00000509621.1:c.1767T>G
NM_032119.3:c.9070T>G	NP_115495.3:p.Tyr3024Asp
NR_003149.1:n.9083T>G
XM_011543675.1:c.9067T>G	XP_011541977.1:p.Tyr3023Asp
XM_011543676.1:c.8989T>G	XP_011541978.1:p.Tyr2997Asp
XM_011543677.1:c.6373T>G	XP_011541979.1:p.Tyr2125Asp
XM_011543678.1:c.9070T>G	XP_011541980.1:p.Tyr3024Asp
XM_011543679.1:c.9070T>G	XP_011541981.1:p.Tyr3024Asp
NM_032119.4:c.9070T>G MANE Select	NP_115495.3:p.Tyr3024Asp
XM_017009963.2:c.9091T>G	XP_016865452.1:p.Tyr3031Asp
XM_017009964.2:c.9088T>G	XP_016865453.1:p.Tyr3030Asp
XM_017009965.1:c.9088T>G	XP_016865454.1:p.Tyr3030Asp
XM_017009966.2:c.9010T>G	XP_016865455.1:p.Tyr3004Asp
XM_017009967.1:c.8995T>G	XP_016865456.1:p.Tyr2999Asp
XM_017009968.2:c.9091T>G	XP_016865457.1:p.Tyr3031Asp
XM_017009969.2:c.9091T>G	XP_016865458.1:p.Tyr3031Asp
XM_017009970.2:c.9091T>G	XP_016865459.1:p.Tyr3031Asp
XM_017009971.2:c.9091T>G	XP_016865460.1:p.Tyr3031Asp
XM_017009972.1:c.2209T>G	XP_016865461.1:p.Tyr737Asp
XM_017009973.1:c.2188T>G	XP_016865462.1:p.Tyr730Asp
XM_017009974.2:c.9091T>G	XP_016865463.1:p.Tyr3031Asp
NR_003149.2:n.9086T>G