Canonical Allele Identifier: CA360392945

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90646093T>G , CM000667.2:g.90646093T>G	GRCh38
NC_000005.9:g.89941910T>G , CM000667.1:g.89941910T>G	GRCh37
NC_000005.8:g.89977666T>G	NCBI36
NG_007083.1:g.92294T>G
NG_007083.2:g.121750T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.3022+2T>G MANE Select	NP_115495.3:n.3022+2T>G
ENST00000405460.9:c.3022+2T>G MANE Select	ENSP00000384582.2:n.3022+2T>G
NM_032119.3:c.3022+2T>G	NP_115495.3:n.3022+2T>G
NR_003149.1:n.3118+2T>G
NR_003149.2:n.3121+2T>G
ENST00000405460.6:c.3022+2T>G	ENSP00000384582.2:n.3022+2T>G
ENST00000504142.1:c.1787+2T>G
ENST00000504142.2:n.1788+2T>G
ENST00000639676.1:n.620+2T>G
ENST00000640403.1:c.325+2T>G	ENSP00000492531.1:n.325+2T>G
XM_011543675.1:c.3022+2T>G	XP_011541977.1:n.3022+2T>G
XM_011543676.1:c.3022+2T>G	XP_011541978.1:n.3022+2T>G
XM_011543677.1:c.325+2T>G	XP_011541979.1:n.325+2T>G
XM_011543678.1:c.3022+2T>G	XP_011541980.1:n.3022+2T>G
XM_011543679.1:c.3022+2T>G	XP_011541981.1:n.3022+2T>G
XM_017009963.2:c.3022+2T>G	XP_016865452.1:n.3022+2T>G
XM_017009964.2:c.3022+2T>G	XP_016865453.1:n.3022+2T>G
XM_017009965.1:c.3019+2T>G	XP_016865454.1:n.3019+2T>G
XM_017009966.2:c.3022+2T>G	XP_016865455.1:n.3022+2T>G
XM_017009967.1:c.2926+2T>G	XP_016865456.1:n.2926+2T>G
XM_017009968.2:c.3022+2T>G	XP_016865457.1:n.3022+2T>G
XM_017009969.2:c.3022+2T>G	XP_016865458.1:n.3022+2T>G
XM_017009970.2:c.3022+2T>G	XP_016865459.1:n.3022+2T>G
XM_017009971.2:c.3022+2T>G	XP_016865460.1:n.3022+2T>G
XM_017009974.2:c.3022+2T>G	XP_016865463.1:n.3022+2T>G