Canonical Allele Identifier: CA445467092

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979888A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684071A>T , CM000667.2:g.90684071A>T	GRCh38
NC_000005.9:g.89979888A>T , CM000667.1:g.89979888A>T	GRCh37
NC_000005.8:g.90015644A>T	NCBI36
NG_007083.1:g.130272A>T
NG_007083.2:g.159728A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6150A>T MANE Select	ENSP00000384582.2:p.Gly2050=
ENST00000639431.1:c.265+7862A>T	ENSP00000491057.1:n.265+7862A>T
ENST00000639473.1:n.1609A>T
ENST00000640012.1:c.165-1709A>T
ENST00000640403.1:c.3441A>T	ENSP00000492531.1:p.Gly1147=
ENST00000640779.1:c.962A>T
ENST00000405460.6:c.6150A>T	ENSP00000384582.2:p.Gly2050=
NM_032119.3:c.6150A>T	NP_115495.3:p.Gly2050=
NR_003149.1:n.6246A>T
XM_011543675.1:c.6147A>T	XP_011541977.1:p.Gly2049=
XM_011543676.1:c.6069A>T	XP_011541978.1:p.Gly2023=
XM_011543677.1:c.3453A>T	XP_011541979.1:p.Gly1151=
XM_011543678.1:c.6150A>T	XP_011541980.1:p.Gly2050=
XM_011543679.1:c.6150A>T	XP_011541981.1:p.Gly2050=
NM_032119.4:c.6150A>T MANE Select	NP_115495.3:p.Gly2050=
XM_017009963.2:c.6150A>T	XP_016865452.1:p.Gly2050=
XM_017009964.2:c.6147A>T	XP_016865453.1:p.Gly2049=
XM_017009965.1:c.6147A>T	XP_016865454.1:p.Gly2049=
XM_017009966.2:c.6069A>T	XP_016865455.1:p.Gly2023=
XM_017009967.1:c.6054A>T	XP_016865456.1:p.Gly2018=
XM_017009968.2:c.6150A>T	XP_016865457.1:p.Gly2050=
XM_017009969.2:c.6150A>T	XP_016865458.1:p.Gly2050=
XM_017009970.2:c.6150A>T	XP_016865459.1:p.Gly2050=
XM_017009971.2:c.6150A>T	XP_016865460.1:p.Gly2050=
XM_017009973.1:c.-650A>T	XP_016865462.1:n.-650A>T
XM_017009974.2:c.6150A>T	XP_016865463.1:p.Gly2050=
NR_003149.2:n.6249A>T