Canonical Allele Identifier: CA1205614167

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293281_168293283delinsAAG , CM000663.2:g.168293281_168293283delinsAAG	GRCh38
NC_000001.10:g.168262519_168262521delinsAAG , CM000663.1:g.168262519_168262521delinsAAG	GRCh37
NC_000001.9:g.166529143_166529145delinsAAG	NCBI36
NG_008244.1:g.17242_17244delinsAAG

Transcript Alleles

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