Canonical Allele Identifier: CA1205614225

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293328_168293332delinsACTGT , CM000663.2:g.168293328_168293332delinsACTGT	GRCh38
NC_000001.10:g.168262566_168262570delinsACTGT , CM000663.1:g.168262566_168262570delinsACTGT	GRCh37
NC_000001.9:g.166529190_166529194delinsACTGT	NCBI36
NG_008244.1:g.17289_17293delinsACTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+50_603+54delinsACTGT MANE Select	ENSP00000356795.3:n.603+50_603+54delinsACTGT
ENST00000367821.7:c.603+50_603+54delinsACTGT	ENSP00000356795.3:n.603+50_603+54delinsACTGT
ENST00000431969.5:c.400+50_400+54delinsACTGT
NM_005149.2:c.603+50_603+54delinsACTGT	NP_005140.1:n.603+50_603+54delinsACTGT
NM_005149.3:c.603+50_603+54delinsACTGT MANE Select	NP_005140.1:n.603+50_603+54delinsACTGT