Canonical Allele Identifier: CA514524920

Gene: TRIOBP

Linked Data

• ClinVar Variation Id: 2498904
• ClinVar RCV Id: RCV003223113
• MyVariant Identifiers: chr22:g.38106550A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37710543A>T , CM000684.2:g.37710543A>T	GRCh38
NC_000022.10:g.38106550A>T , CM000684.1:g.38106550A>T	GRCh37
NC_000022.9:g.36436496A>T	NCBI36
NG_012857.1:g.18556A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644935.1:c.231A>T MANE Select	ENSP00000496394.1:p.Pro77=
ENST00000344404.10:c.231A>T	ENSP00000340312.6:p.Pro77=
ENST00000406386.7:c.231A>T	ENSP00000384312.3:p.Pro77=
ENST00000455236.4:c.1188A>T	ENSP00000477208.1:n.1188A>T
ENST00000492485.5:n.367A>T
NM_001039141.2:c.231A>T	NP_001034230.1:p.Pro77=
NM_001039141.3:c.231A>T MANE Select	NP_001034230.1:p.Pro77=