Canonical Allele Identifier: CA360386933

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90777912C>T , CM000667.2:g.90777912C>T	GRCh38
NC_000005.9:g.90073729C>T , CM000667.1:g.90073729C>T	GRCh37
NC_000005.8:g.90109485C>T	NCBI36
NG_007083.1:g.224113C>T
NG_007083.2:g.253569C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.12535C>T MANE Select	NP_115495.3:p.Arg4179Ter
ENST00000405460.9:c.12535C>T MANE Select	ENSP00000384582.2:p.Arg4179Ter
NM_032119.3:c.12535C>T	NP_115495.3:p.Arg4179Ter
NR_003149.1:n.12548C>T
NR_003149.2:n.12551C>T
ENST00000405460.6:c.12535C>T	ENSP00000384582.2:p.Arg4179Ter
ENST00000425867.3:c.1489C>T	ENSP00000392618.3:p.Arg497Ter
ENST00000639431.1:c.265+101703C>T	ENSP00000491057.1:n.265+101703C>T
ENST00000640464.1:n.2954C>T
ENST00000640729.1:n.1112C>T
XM_011543675.1:c.12532C>T	XP_011541977.1:p.Arg4178Ter
XM_011543676.1:c.12454C>T	XP_011541978.1:p.Arg4152Ter
XM_011543677.1:c.9838C>T	XP_011541979.1:p.Arg3280Ter
XM_011543678.1:c.12535C>T	XP_011541980.1:p.Arg4179Ter
XM_017009963.2:c.12556C>T	XP_016865452.1:p.Arg4186Ter
XM_017009964.2:c.12553C>T	XP_016865453.1:p.Arg4185Ter
XM_017009965.1:c.12553C>T	XP_016865454.1:p.Arg4185Ter
XM_017009966.2:c.12475C>T	XP_016865455.1:p.Arg4159Ter
XM_017009967.1:c.12460C>T	XP_016865456.1:p.Arg4154Ter
XM_017009968.2:c.12556C>T	XP_016865457.1:p.Arg4186Ter
XM_017009969.2:c.12556C>T	XP_016865458.1:p.Arg4186Ter
XM_017009970.2:c.12556C>T	XP_016865459.1:p.Arg4186Ter
XM_017009971.2:c.12556C>T	XP_016865460.1:p.Arg4186Ter
XM_017009972.1:c.5674C>T	XP_016865461.1:p.Arg1892Ter
XM_017009973.1:c.5653C>T	XP_016865462.1:p.Arg1885Ter