Canonical Allele Identifier: CA182556

Gene: TRIOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37757692G>A , CM000684.2:g.37757692G>A	GRCh38
NC_000022.10:g.38153699G>A , CM000684.1:g.38153699G>A	GRCh37
NC_000022.9:g.36483645G>A	NCBI36
NG_012857.1:g.65705G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001039141.3:c.5767G>A MANE Select	NP_001034230.1:p.Ala1923Thr
ENST00000644935.1:c.5767G>A MANE Select	ENSP00000496394.1:p.Ala1923Thr
NM_001039141.2:c.5767G>A	NP_001034230.1:p.Ala1923Thr
NM_007032.5:c.628G>A	NP_008963.3:p.Ala210Thr
NM_138632.2:c.628G>A	NP_619538.2:p.Ala210Thr
ENST00000344404.10:c.*5250G>A	ENSP00000340312.6:n.*5250G>A
ENST00000403663.6:c.628G>A	ENSP00000386026.2:p.Ala210Thr
ENST00000406386.7:c.5767G>A	ENSP00000384312.3:p.Ala1923Thr
ENST00000407319.6:c.628G>A	ENSP00000383913.2:p.Ala210Thr
ENST00000407319.7:c.628G>A	ENSP00000383913.2:p.Ala210Thr
ENST00000413051.2:c.633G>A	ENSP00000400680.2:n.633G>A
ENST00000417857.1:c.415G>A	ENSP00000387881.1:p.Ala139Thr
ENST00000418339.5:c.505G>A	ENSP00000396946.1:p.Ala169Thr
ENST00000428075.5:c.488G>A