Canonical Allele Identifier: CA1205614120

Gene: TBX19

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168293128_168293131delinsTCTC , CM000663.2:g.168293128_168293131delinsTCTC	GRCh38
NC_000001.10:g.168262366_168262369delinsTCTC , CM000663.1:g.168262366_168262369delinsTCTC	GRCh37
NC_000001.9:g.166528990_166528993delinsTCTC	NCBI36
NG_008244.1:g.17089_17092delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367821.8:c.469-16_469-13delinsTCTC MANE Select	ENSP00000356795.3:n.469-16_469-13delinsTCTC
ENST00000367821.7:c.469-16_469-13delinsTCTC	ENSP00000356795.3:n.469-16_469-13delinsTCTC
ENST00000431969.5:c.266-16_266-13delinsTCTC
NM_005149.2:c.469-16_469-13delinsTCTC	NP_005140.1:n.469-16_469-13delinsTCTC
NM_005149.3:c.469-16_469-13delinsTCTC MANE Select	NP_005140.1:n.469-16_469-13delinsTCTC