Canonical Allele Identifier: CA445414348

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90720083A>G , CM000667.2:g.90720083A>G	GRCh38
NC_000005.9:g.90015900A>G , CM000667.1:g.90015900A>G	GRCh37
NC_000005.8:g.90051656A>G	NCBI36
NG_007083.1:g.166284A>G
NG_007083.2:g.195740A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9483A>G MANE Select	NP_115495.3:p.Pro3161=
ENST00000405460.9:c.9483A>G MANE Select	ENSP00000384582.2:p.Pro3161=
NM_032119.3:c.9483A>G	NP_115495.3:p.Pro3161=
NR_003149.1:n.9496A>G
NR_003149.2:n.9499A>G
ENST00000405460.6:c.9483A>G	ENSP00000384582.2:p.Pro3161=
ENST00000509621.1:c.2180A>G
ENST00000639431.1:c.265+43874A>G	ENSP00000491057.1:n.265+43874A>G
ENST00000640374.1:n.2627A>G
ENST00000640779.1:c.4212A>G
XM_011543675.1:c.9480A>G	XP_011541977.1:p.Pro3160=
XM_011543676.1:c.9402A>G	XP_011541978.1:p.Pro3134=
XM_011543677.1:c.6786A>G	XP_011541979.1:p.Pro2262=
XM_011543678.1:c.9483A>G	XP_011541980.1:p.Pro3161=
XM_011543679.1:c.9483A>G	XP_011541981.1:p.Pro3161=
XM_017009963.2:c.9504A>G	XP_016865452.1:p.Pro3168=
XM_017009964.2:c.9501A>G	XP_016865453.1:p.Pro3167=
XM_017009965.1:c.9501A>G	XP_016865454.1:p.Pro3167=
XM_017009966.2:c.9423A>G	XP_016865455.1:p.Pro3141=
XM_017009967.1:c.9408A>G	XP_016865456.1:p.Pro3136=
XM_017009968.2:c.9504A>G	XP_016865457.1:p.Pro3168=
XM_017009969.2:c.9504A>G	XP_016865458.1:p.Pro3168=
XM_017009970.2:c.9504A>G	XP_016865459.1:p.Pro3168=
XM_017009971.2:c.9504A>G	XP_016865460.1:p.Pro3168=
XM_017009972.1:c.2622A>G	XP_016865461.1:p.Pro874=
XM_017009973.1:c.2601A>G	XP_016865462.1:p.Pro867=
XM_017009974.2:c.9504A>G	XP_016865463.1:p.Pro3168=
XR_001742802.1:n.2523-4274T>C
XR_948560.1:n.272-4274T>C