Canonical Allele Identifier: CA10224815

Gene: TRIOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37757713C>T , CM000684.2:g.37757713C>T	GRCh38
NC_000022.10:g.38153720C>T , CM000684.1:g.38153720C>T	GRCh37
NC_000022.9:g.36483666C>T	NCBI36
NG_012857.1:g.65726C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001039141.3:c.5788C>T MANE Select	NP_001034230.1:p.Arg1930Trp
ENST00000644935.1:c.5788C>T MANE Select	ENSP00000496394.1:p.Arg1930Trp
NM_001039141.2:c.5788C>T	NP_001034230.1:p.Arg1930Trp
NM_007032.5:c.649C>T	NP_008963.3:p.Arg217Trp
NM_138632.2:c.649C>T	NP_619538.2:p.Arg217Trp
ENST00000344404.10:c.*5271C>T	ENSP00000340312.6:n.*5271C>T
ENST00000403663.6:c.649C>T	ENSP00000386026.2:p.Arg217Trp
ENST00000406386.7:c.5788C>T	ENSP00000384312.3:p.Arg1930Trp
ENST00000407319.6:c.649C>T	ENSP00000383913.2:p.Arg217Trp
ENST00000407319.7:c.649C>T	ENSP00000383913.2:p.Arg217Trp
ENST00000413051.2:c.654C>T	ENSP00000400680.2:n.654C>T
ENST00000417857.1:c.436C>T	ENSP00000387881.1:p.Arg146Trp
ENST00000418339.5:c.526C>T	ENSP00000396946.1:p.Arg176Trp
ENST00000428075.5:c.509C>T