Canonical Allele Identifier: CA360370978

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90692651-G-T
• MyVariant Identifiers: chr5:g.89988468G>T (hg19) ; chr5:g.90692651G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692651G>T , CM000667.2:g.90692651G>T	GRCh38
NC_000005.9:g.89988468G>T , CM000667.1:g.89988468G>T	GRCh37
NC_000005.8:g.90024224G>T	NCBI36
NG_007083.1:g.138852G>T
NG_007083.2:g.168308G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6998G>T MANE Select	ENSP00000384582.2:p.Gly2333Val
ENST00000639431.1:c.265+16442G>T	ENSP00000491057.1:n.265+16442G>T
ENST00000639473.1:n.2457G>T
ENST00000640012.1:c.805G>T
ENST00000640374.1:n.142G>T
ENST00000640403.1:c.4289G>T	ENSP00000492531.1:p.Gly1430Val
ENST00000640779.1:c.1727G>T
ENST00000405460.6:c.6998G>T	ENSP00000384582.2:p.Gly2333Val
NM_032119.3:c.6998G>T	NP_115495.3:p.Gly2333Val
NR_003149.1:n.7011G>T
XM_011543675.1:c.6995G>T	XP_011541977.1:p.Gly2332Val
XM_011543676.1:c.6917G>T	XP_011541978.1:p.Gly2306Val
XM_011543677.1:c.4301G>T	XP_011541979.1:p.Gly1434Val
XM_011543678.1:c.6998G>T	XP_011541980.1:p.Gly2333Val
XM_011543679.1:c.6998G>T	XP_011541981.1:p.Gly2333Val
NM_032119.4:c.6998G>T MANE Select	NP_115495.3:p.Gly2333Val
XM_017009963.2:c.6998G>T	XP_016865452.1:p.Gly2333Val
XM_017009964.2:c.6995G>T	XP_016865453.1:p.Gly2332Val
XM_017009965.1:c.6995G>T	XP_016865454.1:p.Gly2332Val
XM_017009966.2:c.6917G>T	XP_016865455.1:p.Gly2306Val
XM_017009967.1:c.6902G>T	XP_016865456.1:p.Gly2301Val
XM_017009968.2:c.6998G>T	XP_016865457.1:p.Gly2333Val
XM_017009969.2:c.6998G>T	XP_016865458.1:p.Gly2333Val
XM_017009970.2:c.6998G>T	XP_016865459.1:p.Gly2333Val
XM_017009971.2:c.6998G>T	XP_016865460.1:p.Gly2333Val
XM_017009972.1:c.116G>T	XP_016865461.1:p.Gly39Val
XM_017009973.1:c.116G>T	XP_016865462.1:p.Gly39Val
XM_017009974.2:c.6998G>T	XP_016865463.1:p.Gly2333Val
NR_003149.2:n.7014G>T