Canonical Allele Identifier: CA1205614183
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293290_168293301delinsTGTGTGTGTGTG , CM000663.2:g.168293290_168293301delinsTGTGTGTGTGTG GRCh38
NC_000001.10:g.168262528_168262539delinsTGTGTGTGTGTG , CM000663.1:g.168262528_168262539delinsTGTGTGTGTGTG GRCh37
NC_000001.9:g.166529152_166529163delinsTGTGTGTGTGTG NCBI36
NG_008244.1:g.17251_17262delinsTGTGTGTGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+12_603+23delinsTGTGTGTGTGTG MANE Select ENSP00000356795.3:n.603+12_603+23delinsTGTGTGTGTGTG
ENST00000367821.7:c.603+12_603+23delinsTGTGTGTGTGTG ENSP00000356795.3:n.603+12_603+23delinsTGTGTGTGTGTG
ENST00000431969.5:c.400+12_400+23delinsTGTGTGTGTGTG
NM_005149.2:c.603+12_603+23delinsTGTGTGTGTGTG NP_005140.1:n.603+12_603+23delinsTGTGTGTGTGTG
NM_005149.3:c.603+12_603+23delinsTGTGTGTGTGTG MANE Select NP_005140.1:n.603+12_603+23delinsTGTGTGTGTGTG