Canonical Allele Identifier: CA2531561360
Gene: TBX19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168293291_168293313del , CM000663.2:g.168293291_168293313del GRCh38
NC_000001.10:g.168262529_168262551del , CM000663.1:g.168262529_168262551del GRCh37
NC_000001.9:g.166529153_166529175del NCBI36
NG_008244.1:g.17252_17274del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367821.8:c.603+13_603+35del MANE Select ENSP00000356795.3:n.603+13_603+35del
ENST00000367821.7:c.603+13_603+35del ENSP00000356795.3:n.603+13_603+35del
ENST00000431969.5:c.400+13_400+35del
NM_005149.2:c.603+13_603+35del NP_005140.1:n.603+13_603+35del
NM_005149.3:c.603+13_603+35del MANE Select NP_005140.1:n.603+13_603+35del