Canonical Allele Identifier: CA360371749

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988559G>T (hg19) ; chr5:g.90692742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692742G>T , CM000667.2:g.90692742G>T	GRCh38
NC_000005.9:g.89988559G>T , CM000667.1:g.89988559G>T	GRCh37
NC_000005.8:g.90024315G>T	NCBI36
NG_007083.1:g.138943G>T
NG_007083.2:g.168399G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7089G>T MANE Select	ENSP00000384582.2:p.Glu2363Asp
ENST00000639431.1:c.265+16533G>T	ENSP00000491057.1:n.265+16533G>T
ENST00000639473.1:n.2548G>T
ENST00000640012.1:c.896G>T
ENST00000640374.1:n.233G>T
ENST00000640403.1:c.4380G>T	ENSP00000492531.1:p.Glu1460Asp
ENST00000640779.1:c.1818G>T
ENST00000405460.6:c.7089G>T	ENSP00000384582.2:p.Glu2363Asp
NM_032119.3:c.7089G>T	NP_115495.3:p.Glu2363Asp
NR_003149.1:n.7102G>T
XM_011543675.1:c.7086G>T	XP_011541977.1:p.Glu2362Asp
XM_011543676.1:c.7008G>T	XP_011541978.1:p.Glu2336Asp
XM_011543677.1:c.4392G>T	XP_011541979.1:p.Glu1464Asp
XM_011543678.1:c.7089G>T	XP_011541980.1:p.Glu2363Asp
XM_011543679.1:c.7089G>T	XP_011541981.1:p.Glu2363Asp
NM_032119.4:c.7089G>T MANE Select	NP_115495.3:p.Glu2363Asp
XM_017009963.2:c.7089G>T	XP_016865452.1:p.Glu2363Asp
XM_017009964.2:c.7086G>T	XP_016865453.1:p.Glu2362Asp
XM_017009965.1:c.7086G>T	XP_016865454.1:p.Glu2362Asp
XM_017009966.2:c.7008G>T	XP_016865455.1:p.Glu2336Asp
XM_017009967.1:c.6993G>T	XP_016865456.1:p.Glu2331Asp
XM_017009968.2:c.7089G>T	XP_016865457.1:p.Glu2363Asp
XM_017009969.2:c.7089G>T	XP_016865458.1:p.Glu2363Asp
XM_017009970.2:c.7089G>T	XP_016865459.1:p.Glu2363Asp
XM_017009971.2:c.7089G>T	XP_016865460.1:p.Glu2363Asp
XM_017009972.1:c.207G>T	XP_016865461.1:p.Glu69Asp
XM_017009973.1:c.207G>T	XP_016865462.1:p.Glu69Asp
XM_017009974.2:c.7089G>T	XP_016865463.1:p.Glu2363Asp
NR_003149.2:n.7105G>T