Canonical Allele Identifier: CA138251

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90706255C>T , CM000667.2:g.90706255C>T	GRCh38
NC_000005.9:g.90002072C>T , CM000667.1:g.90002072C>T	GRCh37
NC_000005.8:g.90037828C>T	NCBI36
NG_007083.1:g.152456C>T
NG_007083.2:g.181912C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.8591C>T MANE Select	NP_115495.3:p.Thr2864Met
ENST00000405460.9:c.8591C>T MANE Select	ENSP00000384582.2:p.Thr2864Met
NM_032119.3:c.8591C>T	NP_115495.3:p.Thr2864Met
NR_003149.1:n.8604C>T
NR_003149.2:n.8607C>T
ENST00000405460.6:c.8591C>T	ENSP00000384582.2:p.Thr2864Met
ENST00000509621.1:c.1288C>T
ENST00000639431.1:c.265+30046C>T	ENSP00000491057.1:n.265+30046C>T
ENST00000639473.1:n.4050C>T
ENST00000640012.1:c.2398C>T
ENST00000640374.1:n.1735C>T
ENST00000640403.1:c.5882C>T	ENSP00000492531.1:p.Thr1961Met
ENST00000640779.1:c.3320C>T
XM_011543675.1:c.8588C>T	XP_011541977.1:p.Thr2863Met
XM_011543676.1:c.8510C>T	XP_011541978.1:p.Thr2837Met
XM_011543677.1:c.5894C>T	XP_011541979.1:p.Thr1965Met
XM_011543678.1:c.8591C>T	XP_011541980.1:p.Thr2864Met
XM_011543679.1:c.8591C>T	XP_011541981.1:p.Thr2864Met
XM_017009963.2:c.8612C>T	XP_016865452.1:p.Thr2871Met
XM_017009964.2:c.8609C>T	XP_016865453.1:p.Thr2870Met
XM_017009965.1:c.8609C>T	XP_016865454.1:p.Thr2870Met
XM_017009966.2:c.8531C>T	XP_016865455.1:p.Thr2844Met
XM_017009967.1:c.8516C>T	XP_016865456.1:p.Thr2839Met
XM_017009968.2:c.8612C>T	XP_016865457.1:p.Thr2871Met
XM_017009969.2:c.8612C>T	XP_016865458.1:p.Thr2871Met
XM_017009970.2:c.8612C>T	XP_016865459.1:p.Thr2871Met
XM_017009971.2:c.8612C>T	XP_016865460.1:p.Thr2871Met
XM_017009972.1:c.1730C>T	XP_016865461.1:p.Thr577Met
XM_017009973.1:c.1709C>T	XP_016865462.1:p.Thr570Met
XM_017009974.2:c.8612C>T	XP_016865463.1:p.Thr2871Met