Canonical Allele Identifier: CA360392088

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90002129A>T (hg19) ; chr5:g.90706312A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90706312A>T , CM000667.2:g.90706312A>T	GRCh38
NC_000005.9:g.90002129A>T , CM000667.1:g.90002129A>T	GRCh37
NC_000005.8:g.90037885A>T	NCBI36
NG_007083.1:g.152513A>T
NG_007083.2:g.181969A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.8648A>T MANE Select	ENSP00000384582.2:p.Glu2883Val
ENST00000639431.1:c.265+30103A>T	ENSP00000491057.1:n.265+30103A>T
ENST00000639473.1:n.4107A>T
ENST00000640012.1:c.2455A>T
ENST00000640374.1:n.1792A>T
ENST00000640403.1:c.5939A>T	ENSP00000492531.1:p.Glu1980Val
ENST00000640779.1:c.3377A>T
ENST00000405460.6:c.8648A>T	ENSP00000384582.2:p.Glu2883Val
ENST00000509621.1:c.1345A>T
NM_032119.3:c.8648A>T	NP_115495.3:p.Glu2883Val
NR_003149.1:n.8661A>T
XM_011543675.1:c.8645A>T	XP_011541977.1:p.Glu2882Val
XM_011543676.1:c.8567A>T	XP_011541978.1:p.Glu2856Val
XM_011543677.1:c.5951A>T	XP_011541979.1:p.Glu1984Val
XM_011543678.1:c.8648A>T	XP_011541980.1:p.Glu2883Val
XM_011543679.1:c.8648A>T	XP_011541981.1:p.Glu2883Val
NM_032119.4:c.8648A>T MANE Select	NP_115495.3:p.Glu2883Val
XM_017009963.2:c.8669A>T	XP_016865452.1:p.Glu2890Val
XM_017009964.2:c.8666A>T	XP_016865453.1:p.Glu2889Val
XM_017009965.1:c.8666A>T	XP_016865454.1:p.Glu2889Val
XM_017009966.2:c.8588A>T	XP_016865455.1:p.Glu2863Val
XM_017009967.1:c.8573A>T	XP_016865456.1:p.Glu2858Val
XM_017009968.2:c.8669A>T	XP_016865457.1:p.Glu2890Val
XM_017009969.2:c.8669A>T	XP_016865458.1:p.Glu2890Val
XM_017009970.2:c.8669A>T	XP_016865459.1:p.Glu2890Val
XM_017009971.2:c.8669A>T	XP_016865460.1:p.Glu2890Val
XM_017009972.1:c.1787A>T	XP_016865461.1:p.Glu596Val
XM_017009973.1:c.1766A>T	XP_016865462.1:p.Glu589Val
XM_017009974.2:c.8669A>T	XP_016865463.1:p.Glu2890Val
NR_003149.2:n.8664A>T