Canonical Allele Identifier: CA360371618

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988543T>G (hg19) ; chr5:g.90692726T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692726T>G , CM000667.2:g.90692726T>G	GRCh38
NC_000005.9:g.89988543T>G , CM000667.1:g.89988543T>G	GRCh37
NC_000005.8:g.90024299T>G	NCBI36
NG_007083.1:g.138927T>G
NG_007083.2:g.168383T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7073T>G MANE Select	ENSP00000384582.2:p.Val2358Gly
ENST00000639431.1:c.265+16517T>G	ENSP00000491057.1:n.265+16517T>G
ENST00000639473.1:n.2532T>G
ENST00000640012.1:c.880T>G
ENST00000640374.1:n.217T>G
ENST00000640403.1:c.4364T>G	ENSP00000492531.1:p.Val1455Gly
ENST00000640779.1:c.1802T>G
ENST00000405460.6:c.7073T>G	ENSP00000384582.2:p.Val2358Gly
NM_032119.3:c.7073T>G	NP_115495.3:p.Val2358Gly
NR_003149.1:n.7086T>G
XM_011543675.1:c.7070T>G	XP_011541977.1:p.Val2357Gly
XM_011543676.1:c.6992T>G	XP_011541978.1:p.Val2331Gly
XM_011543677.1:c.4376T>G	XP_011541979.1:p.Val1459Gly
XM_011543678.1:c.7073T>G	XP_011541980.1:p.Val2358Gly
XM_011543679.1:c.7073T>G	XP_011541981.1:p.Val2358Gly
NM_032119.4:c.7073T>G MANE Select	NP_115495.3:p.Val2358Gly
XM_017009963.2:c.7073T>G	XP_016865452.1:p.Val2358Gly
XM_017009964.2:c.7070T>G	XP_016865453.1:p.Val2357Gly
XM_017009965.1:c.7070T>G	XP_016865454.1:p.Val2357Gly
XM_017009966.2:c.6992T>G	XP_016865455.1:p.Val2331Gly
XM_017009967.1:c.6977T>G	XP_016865456.1:p.Val2326Gly
XM_017009968.2:c.7073T>G	XP_016865457.1:p.Val2358Gly
XM_017009969.2:c.7073T>G	XP_016865458.1:p.Val2358Gly
XM_017009970.2:c.7073T>G	XP_016865459.1:p.Val2358Gly
XM_017009971.2:c.7073T>G	XP_016865460.1:p.Val2358Gly
XM_017009972.1:c.191T>G	XP_016865461.1:p.Val64Gly
XM_017009973.1:c.191T>G	XP_016865462.1:p.Val64Gly
XM_017009974.2:c.7073T>G	XP_016865463.1:p.Val2358Gly
NR_003149.2:n.7089T>G