Canonical Allele Identifier: CA561259752

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90724998C>T , CM000667.2:g.90724998C>T	GRCh38
NC_000005.9:g.90020815C>T , CM000667.1:g.90020815C>T	GRCh37
NC_000005.8:g.90056571C>T	NCBI36
NG_007083.1:g.171199C>T
NG_007083.2:g.200655C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.9906+9C>T MANE Select	NP_115495.3:n.9906+9C>T
ENST00000405460.9:c.9906+9C>T MANE Select	ENSP00000384582.2:n.9906+9C>T
NM_032119.3:c.9906+9C>T	NP_115495.3:n.9906+9C>T
NR_003149.1:n.9919+9C>T
NR_003149.2:n.9922+9C>T
ENST00000405460.6:c.9906+9C>T	ENSP00000384582.2:n.9906+9C>T
ENST00000509621.1:c.2603+9C>T
ENST00000639431.1:c.265+48789C>T	ENSP00000491057.1:n.265+48789C>T
ENST00000640374.1:n.3050+9C>T
ENST00000640464.1:n.325+9C>T
ENST00000640779.1:c.4635+9C>T
XM_011543675.1:c.9903+9C>T	XP_011541977.1:n.9903+9C>T
XM_011543676.1:c.9825+9C>T	XP_011541978.1:n.9825+9C>T
XM_011543677.1:c.7209+9C>T	XP_011541979.1:n.7209+9C>T
XM_011543678.1:c.9906+9C>T	XP_011541980.1:n.9906+9C>T
XM_011543679.1:c.9906+9C>T	XP_011541981.1:n.9906+9C>T
XM_017009963.2:c.9927+9C>T	XP_016865452.1:n.9927+9C>T
XM_017009964.2:c.9924+9C>T	XP_016865453.1:n.9924+9C>T
XM_017009965.1:c.9924+9C>T	XP_016865454.1:n.9924+9C>T
XM_017009966.2:c.9846+9C>T	XP_016865455.1:n.9846+9C>T
XM_017009967.1:c.9831+9C>T	XP_016865456.1:n.9831+9C>T
XM_017009968.2:c.9927+9C>T	XP_016865457.1:n.9927+9C>T
XM_017009969.2:c.9927+9C>T	XP_016865458.1:n.9927+9C>T
XM_017009970.2:c.9927+9C>T	XP_016865459.1:n.9927+9C>T
XM_017009971.2:c.9927+9C>T	XP_016865460.1:n.9927+9C>T
XM_017009972.1:c.3045+9C>T	XP_016865461.1:n.3045+9C>T
XM_017009973.1:c.3024+9C>T	XP_016865462.1:n.3024+9C>T
XM_017009974.2:c.9927+9C>T	XP_016865463.1:n.9927+9C>T
XR_001742802.1:n.2523-9189G>A
XR_948560.1:n.272-9189G>A