Canonical Allele Identifier: CA2746547404

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293328_168293329insGTCT , CM000663.2:g.168293328_168293329insGTCT	GRCh38
NC_000001.10:g.168262566_168262567insGTCT , CM000663.1:g.168262566_168262567insGTCT	GRCh37
NC_000001.9:g.166529190_166529191insGTCT	NCBI36
NG_008244.1:g.17289_17290insGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+50_603+51insGTCT MANE Select	ENSP00000356795.3:n.603+50_603+51insGTCT
ENST00000367821.7:c.603+50_603+51insGTCT	ENSP00000356795.3:n.603+50_603+51insGTCT
ENST00000431969.5:c.400+50_400+51insGTCT
NM_005149.2:c.603+50_603+51insGTCT	NP_005140.1:n.603+50_603+51insGTCT
NM_005149.3:c.603+50_603+51insGTCT MANE Select	NP_005140.1:n.603+50_603+51insGTCT