Canonical Allele Identifier: CA360407485

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90040880G>T (hg19) ; chr5:g.90745063G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745063G>T , CM000667.2:g.90745063G>T	GRCh38
NC_000005.9:g.90040880G>T , CM000667.1:g.90040880G>T	GRCh37
NC_000005.8:g.90076636G>T	NCBI36
NG_007083.1:g.191264G>T
NG_007083.2:g.220720G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10567G>T MANE Select	ENSP00000384582.2:p.Gly3523Cys
ENST00000639431.1:c.265+68854G>T	ENSP00000491057.1:n.265+68854G>T
ENST00000640374.1:n.3711G>T
ENST00000640464.1:n.986G>T
ENST00000405460.6:c.10567G>T	ENSP00000384582.2:p.Gly3523Cys
ENST00000509621.1:c.3264G>T
NM_032119.3:c.10567G>T	NP_115495.3:p.Gly3523Cys
NR_003149.1:n.10580G>T
XM_011543675.1:c.10564G>T	XP_011541977.1:p.Gly3522Cys
XM_011543676.1:c.10486G>T	XP_011541978.1:p.Gly3496Cys
XM_011543677.1:c.7870G>T	XP_011541979.1:p.Gly2624Cys
XM_011543678.1:c.10567G>T	XP_011541980.1:p.Gly3523Cys
XM_011543679.1:c.10567G>T	XP_011541981.1:p.Gly3523Cys
NM_032119.4:c.10567G>T MANE Select	NP_115495.3:p.Gly3523Cys
XM_017009963.2:c.10588G>T	XP_016865452.1:p.Gly3530Cys
XM_017009964.2:c.10585G>T	XP_016865453.1:p.Gly3529Cys
XM_017009965.1:c.10585G>T	XP_016865454.1:p.Gly3529Cys
XM_017009966.2:c.10507G>T	XP_016865455.1:p.Gly3503Cys
XM_017009967.1:c.10492G>T	XP_016865456.1:p.Gly3498Cys
XM_017009968.2:c.10588G>T	XP_016865457.1:p.Gly3530Cys
XM_017009969.2:c.10588G>T	XP_016865458.1:p.Gly3530Cys
XM_017009970.2:c.10588G>T	XP_016865459.1:p.Gly3530Cys
XM_017009971.2:c.10588G>T	XP_016865460.1:p.Gly3530Cys
XM_017009972.1:c.3706G>T	XP_016865461.1:p.Gly1236Cys
XM_017009973.1:c.3685G>T	XP_016865462.1:p.Gly1229Cys
XM_017009974.2:c.10588G>T	XP_016865463.1:p.Gly3530Cys
NR_003149.2:n.10583G>T