Canonical Allele Identifier: CA411510222
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38164120G>A (hg19) chr22:g.37768113G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768113G>A , CM000684.2:g.37768113G>A GRCh38
NC_000022.10:g.38164120G>A , CM000684.1:g.38164120G>A GRCh37
NC_000022.9:g.36494066G>A NCBI36
NG_012857.1:g.76126G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.6512G>A MANE Select ENSP00000496394.1:p.Ser2171Asn
ENST00000344404.10:c.*5995G>A ENSP00000340312.6:n.*5995G>A
ENST00000403663.6:c.1373G>A ENSP00000386026.2:p.Ser458Asn
ENST00000406386.7:c.6512G>A ENSP00000384312.3:p.Ser2171Asn
NM_001039141.2:c.6512G>A NP_001034230.1:p.Ser2171Asn
NM_007032.5:c.1373G>A NP_008963.3:p.Ser458Asn
NM_001039141.3:c.6512G>A MANE Select NP_001034230.1:p.Ser2171Asn
Search 100 bp 5'
Search 100 bp 3'