Canonical Allele Identifier: CA3340815

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90745264A>T , CM000667.2:g.90745264A>T	GRCh38
NC_000005.9:g.90041081A>T , CM000667.1:g.90041081A>T	GRCh37
NC_000005.8:g.90076837A>T	NCBI36
NG_007083.1:g.191465A>T
NG_007083.2:g.220921A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10768A>T MANE Select	ENSP00000384582.2:p.Ser3590Cys
ENST00000639431.1:c.265+69055A>T	ENSP00000491057.1:n.265+69055A>T
ENST00000640374.1:n.3912A>T
ENST00000640464.1:n.1187A>T
ENST00000405460.6:c.10768A>T	ENSP00000384582.2:p.Ser3590Cys
ENST00000509621.1:c.3465A>T
NM_032119.3:c.10768A>T	NP_115495.3:p.Ser3590Cys
NR_003149.1:n.10781A>T
XM_011543675.1:c.10765A>T	XP_011541977.1:p.Ser3589Cys
XM_011543676.1:c.10687A>T	XP_011541978.1:p.Ser3563Cys
XM_011543677.1:c.8071A>T	XP_011541979.1:p.Ser2691Cys
XM_011543678.1:c.10768A>T	XP_011541980.1:p.Ser3590Cys
XM_011543679.1:c.10768A>T	XP_011541981.1:p.Arg3590Trp
NM_032119.4:c.10768A>T MANE Select	NP_115495.3:p.Ser3590Cys
XM_017009963.2:c.10789A>T	XP_016865452.1:p.Ser3597Cys
XM_017009964.2:c.10786A>T	XP_016865453.1:p.Ser3596Cys
XM_017009965.1:c.10786A>T	XP_016865454.1:p.Ser3596Cys
XM_017009966.2:c.10708A>T	XP_016865455.1:p.Ser3570Cys
XM_017009967.1:c.10693A>T	XP_016865456.1:p.Ser3565Cys
XM_017009968.2:c.10789A>T	XP_016865457.1:p.Ser3597Cys
XM_017009969.2:c.10789A>T	XP_016865458.1:p.Ser3597Cys
XM_017009970.2:c.10789A>T	XP_016865459.1:p.Ser3597Cys
XM_017009971.2:c.10789A>T	XP_016865460.1:p.Ser3597Cys
XM_017009972.1:c.3907A>T	XP_016865461.1:p.Ser1303Cys
XM_017009973.1:c.3886A>T	XP_016865462.1:p.Ser1296Cys
XM_017009974.2:c.10789A>T	XP_016865463.1:p.Arg3597Trp
NR_003149.2:n.10784A>T