Canonical Allele Identifier: CA2404473272

Gene: TRIOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37710724_37710736delinsCATGCTCCTTGGG , CM000684.2:g.37710724_37710736delinsCATGCTCCTTGGG	GRCh38
NC_000022.10:g.38106731_38106743delinsCATGCTCCTTGGG , CM000684.1:g.38106731_38106743delinsCATGCTCCTTGGG	GRCh37
NC_000022.9:g.36436677_36436689delinsCATGCTCCTTGGG	NCBI36
NG_012857.1:g.18737_18749delinsCATGCTCCTTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644935.1:c.254+158_254+170delinsCATGCTCCTTGGG MANE Select	ENSP00000496394.1:n.254+158_254+170delinsCATGCTCCTTGGG
ENST00000344404.10:c.254+158_254+170delinsCATGCTCCTTGGG	ENSP00000340312.6:n.254+158_254+170delinsCATGCTCCTTGGG
ENST00000406386.7:c.254+158_254+170delinsCATGCTCCTTGGG	ENSP00000384312.3:n.254+158_254+170delinsCATGCTCCTTGGG
ENST00000455236.4:c.1211+158_1211+170delinsCATGCTCCTTGGG	ENSP00000477208.1:n.1211+158_1211+170delinsCATGCTCCTTGGG
ENST00000492485.5:n.390+158_390+170delinsCATGCTCCTTGGG
NM_001039141.2:c.254+158_254+170delinsCATGCTCCTTGGG	NP_001034230.1:n.254+158_254+170delinsCATGCTCCTTGGG
NM_001039141.3:c.254+158_254+170delinsCATGCTCCTTGGG MANE Select	NP_001034230.1:n.254+158_254+170delinsCATGCTCCTTGGG