Canonical Allele Identifier: CA2580073727

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90683355C>T , CM000667.2:g.90683355C>T	GRCh38
NC_000005.9:g.89979172C>T , CM000667.1:g.89979172C>T	GRCh37
NC_000005.8:g.90014928C>T	NCBI36
NG_007083.1:g.129556C>T
NG_007083.2:g.159012C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.5665-231C>T MANE Select	NP_115495.3:n.5665-231C>T
ENST00000405460.9:c.5665-231C>T MANE Select	ENSP00000384582.2:n.5665-231C>T
NM_032119.3:c.5665-231C>T	NP_115495.3:n.5665-231C>T
NR_003149.1:n.5761-231C>T
NR_003149.2:n.5764-231C>T
ENST00000405460.6:c.5665-231C>T	ENSP00000384582.2:n.5665-231C>T
ENST00000639431.1:c.265+7146C>T	ENSP00000491057.1:n.265+7146C>T
ENST00000639473.1:n.1124-231C>T
ENST00000640012.1:c.164+1901C>T
ENST00000640403.1:c.2956-231C>T	ENSP00000492531.1:n.2956-231C>T
ENST00000640779.1:c.477-231C>T
XM_011543675.1:c.5662-231C>T	XP_011541977.1:n.5662-231C>T
XM_011543676.1:c.5584-231C>T	XP_011541978.1:n.5584-231C>T
XM_011543677.1:c.2968-231C>T	XP_011541979.1:n.2968-231C>T
XM_011543678.1:c.5665-231C>T	XP_011541980.1:n.5665-231C>T
XM_011543679.1:c.5665-231C>T	XP_011541981.1:n.5665-231C>T
XM_017009963.2:c.5665-231C>T	XP_016865452.1:n.5665-231C>T
XM_017009964.2:c.5662-231C>T	XP_016865453.1:n.5662-231C>T
XM_017009965.1:c.5662-231C>T	XP_016865454.1:n.5662-231C>T
XM_017009966.2:c.5584-231C>T	XP_016865455.1:n.5584-231C>T
XM_017009967.1:c.5569-231C>T	XP_016865456.1:n.5569-231C>T
XM_017009968.2:c.5665-231C>T	XP_016865457.1:n.5665-231C>T
XM_017009969.2:c.5665-231C>T	XP_016865458.1:n.5665-231C>T
XM_017009970.2:c.5665-231C>T	XP_016865459.1:n.5665-231C>T
XM_017009971.2:c.5665-231C>T	XP_016865460.1:n.5665-231C>T
XM_017009973.1:c.-1135-231C>T	XP_016865462.1:n.-1135-231C>T
XM_017009974.2:c.5665-231C>T	XP_016865463.1:n.5665-231C>T