Canonical Allele Identifier: CA360396274

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008174A>T (hg19) ; chr5:g.90712357A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712357A>T , CM000667.2:g.90712357A>T	GRCh38
NC_000005.9:g.90008174A>T , CM000667.1:g.90008174A>T	GRCh37
NC_000005.8:g.90043930A>T	NCBI36
NG_007083.1:g.158558A>T
NG_007083.2:g.188014A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9113A>T MANE Select	ENSP00000384582.2:p.Glu3038Val
ENST00000639431.1:c.265+36148A>T	ENSP00000491057.1:n.265+36148A>T
ENST00000639473.1:n.4572A>T
ENST00000640012.1:c.2920A>T
ENST00000640374.1:n.2257A>T
ENST00000640779.1:c.3842A>T
ENST00000405460.6:c.9113A>T	ENSP00000384582.2:p.Glu3038Val
ENST00000509621.1:c.1810A>T
NM_032119.3:c.9113A>T	NP_115495.3:p.Glu3038Val
NR_003149.1:n.9126A>T
XM_011543675.1:c.9110A>T	XP_011541977.1:p.Glu3037Val
XM_011543676.1:c.9032A>T	XP_011541978.1:p.Glu3011Val
XM_011543677.1:c.6416A>T	XP_011541979.1:p.Glu2139Val
XM_011543678.1:c.9113A>T	XP_011541980.1:p.Glu3038Val
XM_011543679.1:c.9113A>T	XP_011541981.1:p.Glu3038Val
NM_032119.4:c.9113A>T MANE Select	NP_115495.3:p.Glu3038Val
XM_017009963.2:c.9134A>T	XP_016865452.1:p.Glu3045Val
XM_017009964.2:c.9131A>T	XP_016865453.1:p.Glu3044Val
XM_017009965.1:c.9131A>T	XP_016865454.1:p.Glu3044Val
XM_017009966.2:c.9053A>T	XP_016865455.1:p.Glu3018Val
XM_017009967.1:c.9038A>T	XP_016865456.1:p.Glu3013Val
XM_017009968.2:c.9134A>T	XP_016865457.1:p.Glu3045Val
XM_017009969.2:c.9134A>T	XP_016865458.1:p.Glu3045Val
XM_017009970.2:c.9134A>T	XP_016865459.1:p.Glu3045Val
XM_017009971.2:c.9134A>T	XP_016865460.1:p.Glu3045Val
XM_017009972.1:c.2252A>T	XP_016865461.1:p.Glu751Val
XM_017009973.1:c.2231A>T	XP_016865462.1:p.Glu744Val
XM_017009974.2:c.9134A>T	XP_016865463.1:p.Glu3045Val
NR_003149.2:n.9129A>T