Canonical Allele Identifier: CA360408908

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90041443A>T (hg19) ; chr5:g.90745626A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745626A>T , CM000667.2:g.90745626A>T	GRCh38
NC_000005.9:g.90041443A>T , CM000667.1:g.90041443A>T	GRCh37
NC_000005.8:g.90077199A>T	NCBI36
NG_007083.1:g.191827A>T
NG_007083.2:g.221283A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10805A>T MANE Select	ENSP00000384582.2:p.Glu3602Val
ENST00000639431.1:c.265+69417A>T	ENSP00000491057.1:n.265+69417A>T
ENST00000640374.1:n.3949A>T
ENST00000640464.1:n.1224A>T
ENST00000405460.6:c.10805A>T	ENSP00000384582.2:p.Glu3602Val
ENST00000509621.1:c.3502A>T
NM_032119.3:c.10805A>T	NP_115495.3:p.Glu3602Val
NR_003149.1:n.10818A>T
XM_011543675.1:c.10802A>T	XP_011541977.1:p.Glu3601Val
XM_011543676.1:c.10724A>T	XP_011541978.1:p.Glu3575Val
XM_011543677.1:c.8108A>T	XP_011541979.1:p.Glu2703Val
XM_011543678.1:c.10805A>T	XP_011541980.1:p.Glu3602Val
XM_011543679.1:c.*27A>T	XP_011541981.1:n.*27A>T
NM_032119.4:c.10805A>T MANE Select	NP_115495.3:p.Glu3602Val
XM_017009963.2:c.10826A>T	XP_016865452.1:p.Glu3609Val
XM_017009964.2:c.10823A>T	XP_016865453.1:p.Glu3608Val
XM_017009965.1:c.10823A>T	XP_016865454.1:p.Glu3608Val
XM_017009966.2:c.10745A>T	XP_016865455.1:p.Glu3582Val
XM_017009967.1:c.10730A>T	XP_016865456.1:p.Glu3577Val
XM_017009968.2:c.10826A>T	XP_016865457.1:p.Glu3609Val
XM_017009969.2:c.10826A>T	XP_016865458.1:p.Glu3609Val
XM_017009970.2:c.10826A>T	XP_016865459.1:p.Glu3609Val
XM_017009971.2:c.10826A>T	XP_016865460.1:p.Glu3609Val
XM_017009972.1:c.3944A>T	XP_016865461.1:p.Glu1315Val
XM_017009973.1:c.3923A>T	XP_016865462.1:p.Glu1308Val
XM_017009974.2:c.*27A>T	XP_016865463.1:n.*27A>T
NR_003149.2:n.10821A>T