Canonical Allele Identifier: CA514525520
Gene: TRIOBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.38111904C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715897C>G , CM000684.2:g.37715897C>G GRCh38
NC_000022.10:g.38111904C>G , CM000684.1:g.38111904C>G GRCh37
NC_000022.9:g.36441850C>G NCBI36
NG_012857.1:g.23910C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.591C>G MANE Select ENSP00000496394.1:p.Ser197=
ENST00000344404.10:c.*74C>G ENSP00000340312.6:n.*74C>G
ENST00000406386.7:c.591C>G ENSP00000384312.3:p.Ser197=
ENST00000455236.4:c.1548C>G ENSP00000477208.1:n.1548C>G
ENST00000492485.5:n.525C>G
NM_001039141.2:c.591C>G NP_001034230.1:p.Ser197=
NM_001039141.3:c.591C>G MANE Select NP_001034230.1:p.Ser197=