Canonical Allele Identifier: CA3338977

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90643885C>T , CM000667.2:g.90643885C>T	GRCh38
NC_000005.9:g.89939702C>T , CM000667.1:g.89939702C>T	GRCh37
NC_000005.8:g.89975458C>T	NCBI36
NG_007083.1:g.90086C>T
NG_007083.2:g.119542C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032119.4:c.2636C>T MANE Select	NP_115495.3:p.Thr879Met
ENST00000405460.9:c.2636C>T MANE Select	ENSP00000384582.2:p.Thr879Met
NM_032119.3:c.2636C>T	NP_115495.3:p.Thr879Met
NR_003149.1:n.2732C>T
NR_003149.2:n.2735C>T
ENST00000405460.6:c.2636C>T	ENSP00000384582.2:p.Thr879Met
ENST00000504142.1:c.1401C>T
ENST00000504142.2:n.1402C>T
ENST00000512205.1:n.546C>T
ENST00000639676.1:n.234C>T
ENST00000640403.1:c.-62C>T	ENSP00000492531.1:n.-62C>T
XM_011543675.1:c.2636C>T	XP_011541977.1:p.Thr879Met
XM_011543676.1:c.2636C>T	XP_011541978.1:p.Thr879Met
XM_011543677.1:c.-62C>T	XP_011541979.1:n.-62C>T
XM_011543678.1:c.2636C>T	XP_011541980.1:p.Thr879Met
XM_011543679.1:c.2636C>T	XP_011541981.1:p.Thr879Met
XM_017009963.2:c.2636C>T	XP_016865452.1:p.Thr879Met
XM_017009964.2:c.2636C>T	XP_016865453.1:p.Thr879Met
XM_017009965.1:c.2633C>T	XP_016865454.1:p.Thr878Met
XM_017009966.2:c.2636C>T	XP_016865455.1:p.Thr879Met
XM_017009967.1:c.2540C>T	XP_016865456.1:p.Thr847Met
XM_017009968.2:c.2636C>T	XP_016865457.1:p.Thr879Met
XM_017009969.2:c.2636C>T	XP_016865458.1:p.Thr879Met
XM_017009970.2:c.2636C>T	XP_016865459.1:p.Thr879Met
XM_017009971.2:c.2636C>T	XP_016865460.1:p.Thr879Met
XM_017009974.2:c.2636C>T	XP_016865463.1:p.Thr879Met