Canonical Allele Identifier: CA3339768

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90685887C>T , CM000667.2:g.90685887C>T	GRCh38
NC_000005.9:g.89981704C>T , CM000667.1:g.89981704C>T	GRCh37
NC_000005.8:g.90017460C>T	NCBI36
NG_007083.1:g.132088C>T
NG_007083.2:g.161544C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.6382C>T MANE Select	NP_115495.3:p.Arg2128Ter
ENST00000405460.9:c.6382C>T MANE Select	ENSP00000384582.2:p.Arg2128Ter
NM_032119.3:c.6382C>T	NP_115495.3:p.Arg2128Ter
NR_003149.1:n.6478C>T
NR_003149.2:n.6481C>T
ENST00000405460.6:c.6382C>T	ENSP00000384582.2:p.Arg2128Ter
ENST00000639431.1:c.265+9678C>T	ENSP00000491057.1:n.265+9678C>T
ENST00000639473.1:n.1841C>T
ENST00000640012.1:c.272C>T
ENST00000640403.1:c.3673C>T	ENSP00000492531.1:p.Arg1225Ter
ENST00000640779.1:c.1194C>T
XM_011543675.1:c.6379C>T	XP_011541977.1:p.Arg2127Ter
XM_011543676.1:c.6301C>T	XP_011541978.1:p.Arg2101Ter
XM_011543677.1:c.3685C>T	XP_011541979.1:p.Arg1229Ter
XM_011543678.1:c.6382C>T	XP_011541980.1:p.Arg2128Ter
XM_011543679.1:c.6382C>T	XP_011541981.1:p.Arg2128Ter
XM_017009963.2:c.6382C>T	XP_016865452.1:p.Arg2128Ter
XM_017009964.2:c.6379C>T	XP_016865453.1:p.Arg2127Ter
XM_017009965.1:c.6379C>T	XP_016865454.1:p.Arg2127Ter
XM_017009966.2:c.6301C>T	XP_016865455.1:p.Arg2101Ter
XM_017009967.1:c.6286C>T	XP_016865456.1:p.Arg2096Ter
XM_017009968.2:c.6382C>T	XP_016865457.1:p.Arg2128Ter
XM_017009969.2:c.6382C>T	XP_016865458.1:p.Arg2128Ter
XM_017009970.2:c.6382C>T	XP_016865459.1:p.Arg2128Ter
XM_017009971.2:c.6382C>T	XP_016865460.1:p.Arg2128Ter
XM_017009973.1:c.-418C>T	XP_016865462.1:n.-418C>T
XM_017009974.2:c.6382C>T	XP_016865463.1:p.Arg2128Ter