Canonical Allele Identifier: CA360413361

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90683697C>T , CM000667.2:g.90683697C>T	GRCh38
NC_000005.9:g.89979514C>T , CM000667.1:g.89979514C>T	GRCh37
NC_000005.8:g.90015270C>T	NCBI36
NG_007083.1:g.129898C>T
NG_007083.2:g.159354C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.5776C>T MANE Select	NP_115495.3:p.Gln1926Ter
ENST00000405460.9:c.5776C>T MANE Select	ENSP00000384582.2:p.Gln1926Ter
NM_032119.3:c.5776C>T	NP_115495.3:p.Gln1926Ter
NR_003149.1:n.5872C>T
NR_003149.2:n.5875C>T
ENST00000405460.6:c.5776C>T	ENSP00000384582.2:p.Gln1926Ter
ENST00000639431.1:c.265+7488C>T	ENSP00000491057.1:n.265+7488C>T
ENST00000639473.1:n.1235C>T
ENST00000640012.1:c.165-2083C>T
ENST00000640403.1:c.3067C>T	ENSP00000492531.1:p.Gln1023Ter
ENST00000640779.1:c.588C>T
XM_011543675.1:c.5773C>T	XP_011541977.1:p.Gln1925Ter
XM_011543676.1:c.5695C>T	XP_011541978.1:p.Gln1899Ter
XM_011543677.1:c.3079C>T	XP_011541979.1:p.Gln1027Ter
XM_011543678.1:c.5776C>T	XP_011541980.1:p.Gln1926Ter
XM_011543679.1:c.5776C>T	XP_011541981.1:p.Gln1926Ter
XM_017009963.2:c.5776C>T	XP_016865452.1:p.Gln1926Ter
XM_017009964.2:c.5773C>T	XP_016865453.1:p.Gln1925Ter
XM_017009965.1:c.5773C>T	XP_016865454.1:p.Gln1925Ter
XM_017009966.2:c.5695C>T	XP_016865455.1:p.Gln1899Ter
XM_017009967.1:c.5680C>T	XP_016865456.1:p.Gln1894Ter
XM_017009968.2:c.5776C>T	XP_016865457.1:p.Gln1926Ter
XM_017009969.2:c.5776C>T	XP_016865458.1:p.Gln1926Ter
XM_017009970.2:c.5776C>T	XP_016865459.1:p.Gln1926Ter
XM_017009971.2:c.5776C>T	XP_016865460.1:p.Gln1926Ter
XM_017009973.1:c.-1024C>T	XP_016865462.1:n.-1024C>T
XM_017009974.2:c.5776C>T	XP_016865463.1:p.Gln1926Ter