Canonical Allele Identifier: CA411487081
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1329573714

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733311G>T , CM000684.2:g.37733311G>T GRCh38
NC_000022.10:g.38129318G>T , CM000684.1:g.38129318G>T GRCh37
NC_000022.9:g.36459264G>T NCBI36
NG_012857.1:g.41324G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3961G>T MANE Select ENSP00000496394.1:p.Ala1321Ser
ENST00000344404.10:c.*3444G>T ENSP00000340312.6:n.*3444G>T
ENST00000406386.7:c.3961G>T ENSP00000384312.3:p.Ala1321Ser
NM_001039141.2:c.3961G>T NP_001034230.1:p.Ala1321Ser
XM_011530646.1:c.512-2952C>A XP_011528948.1:n.512-2952C>A
NM_001039141.3:c.3961G>T MANE Select NP_001034230.1:p.Ala1321Ser