Canonical Allele Identifier: CA1205614321

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293531_168293534delinsACTC , CM000663.2:g.168293531_168293534delinsACTC	GRCh38
NC_000001.10:g.168262769_168262772delinsACTC , CM000663.1:g.168262769_168262772delinsACTC	GRCh37
NC_000001.9:g.166529393_166529396delinsACTC	NCBI36
NG_008244.1:g.17492_17495delinsACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.603+253_603+256delinsACTC MANE Select	ENSP00000356795.3:n.603+253_603+256delinsACTC
ENST00000367821.7:c.603+253_603+256delinsACTC	ENSP00000356795.3:n.603+253_603+256delinsACTC
ENST00000431969.5:c.400+253_400+256delinsACTC
NM_005149.2:c.603+253_603+256delinsACTC	NP_005140.1:n.603+253_603+256delinsACTC
NM_005149.3:c.603+253_603+256delinsACTC MANE Select	NP_005140.1:n.603+253_603+256delinsACTC