Canonical Allele Identifier: CA360396313

Gene: ADGRV1

Linked Data

• COSMIC: COSM4846708
• MyVariant Identifiers: chr5:g.90008191C>G (hg19) ; chr5:g.90712374C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712374C>G , CM000667.2:g.90712374C>G	GRCh38
NC_000005.9:g.90008191C>G , CM000667.1:g.90008191C>G	GRCh37
NC_000005.8:g.90043947C>G	NCBI36
NG_007083.1:g.158575C>G
NG_007083.2:g.188031C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9130C>G MANE Select	ENSP00000384582.2:p.Gln3044Glu
ENST00000639431.1:c.265+36165C>G	ENSP00000491057.1:n.265+36165C>G
ENST00000639473.1:n.4589C>G
ENST00000640012.1:c.2937C>G
ENST00000640374.1:n.2274C>G
ENST00000640779.1:c.3859C>G
ENST00000405460.6:c.9130C>G	ENSP00000384582.2:p.Gln3044Glu
ENST00000509621.1:c.1827C>G
NM_032119.3:c.9130C>G	NP_115495.3:p.Gln3044Glu
NR_003149.1:n.9143C>G
XM_011543675.1:c.9127C>G	XP_011541977.1:p.Gln3043Glu
XM_011543676.1:c.9049C>G	XP_011541978.1:p.Gln3017Glu
XM_011543677.1:c.6433C>G	XP_011541979.1:p.Gln2145Glu
XM_011543678.1:c.9130C>G	XP_011541980.1:p.Gln3044Glu
XM_011543679.1:c.9130C>G	XP_011541981.1:p.Gln3044Glu
NM_032119.4:c.9130C>G MANE Select	NP_115495.3:p.Gln3044Glu
XM_017009963.2:c.9151C>G	XP_016865452.1:p.Gln3051Glu
XM_017009964.2:c.9148C>G	XP_016865453.1:p.Gln3050Glu
XM_017009965.1:c.9148C>G	XP_016865454.1:p.Gln3050Glu
XM_017009966.2:c.9070C>G	XP_016865455.1:p.Gln3024Glu
XM_017009967.1:c.9055C>G	XP_016865456.1:p.Gln3019Glu
XM_017009968.2:c.9151C>G	XP_016865457.1:p.Gln3051Glu
XM_017009969.2:c.9151C>G	XP_016865458.1:p.Gln3051Glu
XM_017009970.2:c.9151C>G	XP_016865459.1:p.Gln3051Glu
XM_017009971.2:c.9151C>G	XP_016865460.1:p.Gln3051Glu
XM_017009972.1:c.2269C>G	XP_016865461.1:p.Gln757Glu
XM_017009973.1:c.2248C>G	XP_016865462.1:p.Gln750Glu
XM_017009974.2:c.9151C>G	XP_016865463.1:p.Gln3051Glu
NR_003149.2:n.9146C>G