Canonical Allele Identifier: CA514524909

Gene: TRIOBP

Linked Data

• MyVariant Identifiers: chr22:g.38106532C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37710525C>T , CM000684.2:g.37710525C>T	GRCh38
NC_000022.10:g.38106532C>T , CM000684.1:g.38106532C>T	GRCh37
NC_000022.9:g.36436478C>T	NCBI36
NG_012857.1:g.18538C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644935.1:c.213C>T MANE Select	ENSP00000496394.1:p.Cys71=
ENST00000344404.10:c.213C>T	ENSP00000340312.6:p.Cys71=
ENST00000406386.7:c.213C>T	ENSP00000384312.3:p.Cys71=
ENST00000455236.4:c.1170C>T	ENSP00000477208.1:n.1170C>T
ENST00000492485.5:n.349C>T
NM_001039141.2:c.213C>T	NP_001034230.1:p.Cys71=
NM_001039141.3:c.213C>T MANE Select	NP_001034230.1:p.Cys71=