Canonical Allele Identifier: CA1205614188

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293290_168293299delinsTGTGTGTGTG , CM000663.2:g.168293290_168293299delinsTGTGTGTGTG	GRCh38
NC_000001.10:g.168262528_168262537delinsTGTGTGTGTG , CM000663.1:g.168262528_168262537delinsTGTGTGTGTG	GRCh37
NC_000001.9:g.166529152_166529161delinsTGTGTGTGTG	NCBI36
NG_008244.1:g.17251_17260delinsTGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+12_603+21delinsTGTGTGTGTG MANE Select	ENSP00000356795.3:n.603+12_603+21delinsTGTGTGTGTG
ENST00000367821.7:c.603+12_603+21delinsTGTGTGTGTG	ENSP00000356795.3:n.603+12_603+21delinsTGTGTGTGTG
ENST00000431969.5:c.400+12_400+21delinsTGTGTGTGTG
NM_005149.2:c.603+12_603+21delinsTGTGTGTGTG	NP_005140.1:n.603+12_603+21delinsTGTGTGTGTG
NM_005149.3:c.603+12_603+21delinsTGTGTGTGTG MANE Select	NP_005140.1:n.603+12_603+21delinsTGTGTGTGTG