Canonical Allele Identifier: CA360414232

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979887G>T (hg19) ; chr5:g.90684070G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684070G>T , CM000667.2:g.90684070G>T	GRCh38
NC_000005.9:g.89979887G>T , CM000667.1:g.89979887G>T	GRCh37
NC_000005.8:g.90015643G>T	NCBI36
NG_007083.1:g.130271G>T
NG_007083.2:g.159727G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6149G>T MANE Select	ENSP00000384582.2:p.Gly2050Val
ENST00000639431.1:c.265+7861G>T	ENSP00000491057.1:n.265+7861G>T
ENST00000639473.1:n.1608G>T
ENST00000640012.1:c.165-1710G>T
ENST00000640403.1:c.3440G>T	ENSP00000492531.1:p.Gly1147Val
ENST00000640779.1:c.961G>T
ENST00000405460.6:c.6149G>T	ENSP00000384582.2:p.Gly2050Val
NM_032119.3:c.6149G>T	NP_115495.3:p.Gly2050Val
NR_003149.1:n.6245G>T
XM_011543675.1:c.6146G>T	XP_011541977.1:p.Gly2049Val
XM_011543676.1:c.6068G>T	XP_011541978.1:p.Gly2023Val
XM_011543677.1:c.3452G>T	XP_011541979.1:p.Gly1151Val
XM_011543678.1:c.6149G>T	XP_011541980.1:p.Gly2050Val
XM_011543679.1:c.6149G>T	XP_011541981.1:p.Gly2050Val
NM_032119.4:c.6149G>T MANE Select	NP_115495.3:p.Gly2050Val
XM_017009963.2:c.6149G>T	XP_016865452.1:p.Gly2050Val
XM_017009964.2:c.6146G>T	XP_016865453.1:p.Gly2049Val
XM_017009965.1:c.6146G>T	XP_016865454.1:p.Gly2049Val
XM_017009966.2:c.6068G>T	XP_016865455.1:p.Gly2023Val
XM_017009967.1:c.6053G>T	XP_016865456.1:p.Gly2018Val
XM_017009968.2:c.6149G>T	XP_016865457.1:p.Gly2050Val
XM_017009969.2:c.6149G>T	XP_016865458.1:p.Gly2050Val
XM_017009970.2:c.6149G>T	XP_016865459.1:p.Gly2050Val
XM_017009971.2:c.6149G>T	XP_016865460.1:p.Gly2050Val
XM_017009973.1:c.-651G>T	XP_016865462.1:n.-651G>T
XM_017009974.2:c.6149G>T	XP_016865463.1:p.Gly2050Val
NR_003149.2:n.6248G>T