Canonical Allele Identifier: CA360409086

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041484G>T (hg19) ; chr5:g.90745667G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745667G>T , CM000667.2:g.90745667G>T	GRCh38
NC_000005.9:g.90041484G>T , CM000667.1:g.90041484G>T	GRCh37
NC_000005.8:g.90077240G>T	NCBI36
NG_007083.1:g.191868G>T
NG_007083.2:g.221324G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10846G>T MANE Select	ENSP00000384582.2:p.Glu3616Ter
ENST00000639431.1:c.265+69458G>T	ENSP00000491057.1:n.265+69458G>T
ENST00000640374.1:n.3990G>T
ENST00000640464.1:n.1265G>T
ENST00000405460.6:c.10846G>T	ENSP00000384582.2:p.Glu3616Ter
ENST00000509621.1:c.3543G>T
NM_032119.3:c.10846G>T	NP_115495.3:p.Glu3616Ter
NR_003149.1:n.10859G>T
XM_011543675.1:c.10843G>T	XP_011541977.1:p.Glu3615Ter
XM_011543676.1:c.10765G>T	XP_011541978.1:p.Glu3589Ter
XM_011543677.1:c.8149G>T	XP_011541979.1:p.Glu2717Ter
XM_011543678.1:c.10846G>T	XP_011541980.1:p.Glu3616Ter
XM_011543679.1:c.*68G>T	XP_011541981.1:n.*68G>T
NM_032119.4:c.10846G>T MANE Select	NP_115495.3:p.Glu3616Ter
XM_017009963.2:c.10867G>T	XP_016865452.1:p.Glu3623Ter
XM_017009964.2:c.10864G>T	XP_016865453.1:p.Glu3622Ter
XM_017009965.1:c.10864G>T	XP_016865454.1:p.Glu3622Ter
XM_017009966.2:c.10786G>T	XP_016865455.1:p.Glu3596Ter
XM_017009967.1:c.10771G>T	XP_016865456.1:p.Glu3591Ter
XM_017009968.2:c.10867G>T	XP_016865457.1:p.Glu3623Ter
XM_017009969.2:c.10867G>T	XP_016865458.1:p.Glu3623Ter
XM_017009970.2:c.10867G>T	XP_016865459.1:p.Glu3623Ter
XM_017009971.2:c.10867G>T	XP_016865460.1:p.Glu3623Ter
XM_017009972.1:c.3985G>T	XP_016865461.1:p.Glu1329Ter
XM_017009973.1:c.3964G>T	XP_016865462.1:p.Glu1322Ter
XM_017009974.2:c.*68G>T	XP_016865463.1:n.*68G>T
NR_003149.2:n.10862G>T