Canonical Allele Identifier: CA360397681

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012503C>G (hg19) ; chr5:g.90716686C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716686C>G , CM000667.2:g.90716686C>G	GRCh38
NC_000005.9:g.90012503C>G , CM000667.1:g.90012503C>G	GRCh37
NC_000005.8:g.90048259C>G	NCBI36
NG_007083.1:g.162887C>G
NG_007083.2:g.192343C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9404C>G MANE Select	ENSP00000384582.2:p.Pro3135Arg
ENST00000639431.1:c.265+40477C>G	ENSP00000491057.1:n.265+40477C>G
ENST00000639473.1:n.4863C>G
ENST00000640012.1:c.3211C>G
ENST00000640374.1:n.2548C>G
ENST00000640779.1:c.4133C>G
ENST00000405460.6:c.9404C>G	ENSP00000384582.2:p.Pro3135Arg
ENST00000509621.1:c.2101C>G
NM_032119.3:c.9404C>G	NP_115495.3:p.Pro3135Arg
NR_003149.1:n.9417C>G
XM_011543675.1:c.9401C>G	XP_011541977.1:p.Pro3134Arg
XM_011543676.1:c.9323C>G	XP_011541978.1:p.Pro3108Arg
XM_011543677.1:c.6707C>G	XP_011541979.1:p.Pro2236Arg
XM_011543678.1:c.9404C>G	XP_011541980.1:p.Pro3135Arg
XM_011543679.1:c.9404C>G	XP_011541981.1:p.Pro3135Arg
XR_948560.1:n.272-877G>C
NM_032119.4:c.9404C>G MANE Select	NP_115495.3:p.Pro3135Arg
XM_017009963.2:c.9425C>G	XP_016865452.1:p.Pro3142Arg
XM_017009964.2:c.9422C>G	XP_016865453.1:p.Pro3141Arg
XM_017009965.1:c.9422C>G	XP_016865454.1:p.Pro3141Arg
XM_017009966.2:c.9344C>G	XP_016865455.1:p.Pro3115Arg
XM_017009967.1:c.9329C>G	XP_016865456.1:p.Pro3110Arg
XM_017009968.2:c.9425C>G	XP_016865457.1:p.Pro3142Arg
XM_017009969.2:c.9425C>G	XP_016865458.1:p.Pro3142Arg
XM_017009970.2:c.9425C>G	XP_016865459.1:p.Pro3142Arg
XM_017009971.2:c.9425C>G	XP_016865460.1:p.Pro3142Arg
XM_017009972.1:c.2543C>G	XP_016865461.1:p.Pro848Arg
XM_017009973.1:c.2522C>G	XP_016865462.1:p.Pro841Arg
XM_017009974.2:c.9425C>G	XP_016865463.1:p.Pro3142Arg
XR_001742802.1:n.2523-877G>C
NR_003149.2:n.9420C>G