Canonical Allele Identifier: CA1205614219
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293325_168293329delinsGTAAC , CM000663.2:g.168293325_168293329delinsGTAAC GRCh38
NC_000001.10:g.168262563_168262567delinsGTAAC , CM000663.1:g.168262563_168262567delinsGTAAC GRCh37
NC_000001.9:g.166529187_166529191delinsGTAAC NCBI36
NG_008244.1:g.17286_17290delinsGTAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+47_603+51delinsGTAAC MANE Select ENSP00000356795.3:n.603+47_603+51delinsGTAAC
ENST00000367821.7:c.603+47_603+51delinsGTAAC ENSP00000356795.3:n.603+47_603+51delinsGTAAC
ENST00000431969.5:c.400+47_400+51delinsGTAAC
NM_005149.2:c.603+47_603+51delinsGTAAC NP_005140.1:n.603+47_603+51delinsGTAAC
NM_005149.3:c.603+47_603+51delinsGTAAC MANE Select NP_005140.1:n.603+47_603+51delinsGTAAC