Canonical Allele Identifier: CA2147720284

Gene: TGFB3 IFT43

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75962951A= , CM000676.2:g.75962951A=	GRCh38
NC_000014.8:g.76429294A= , CM000676.1:g.76429294A=	GRCh37
NC_000014.7:g.75499047A=	NCBI36
NG_011715.1:g.23799T= , LRG_399:g.23799T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000238682.8:c.926+365T= (TGFB3) MANE Select	ENSP00000238682.3:n.926+365T=
ENST00000556674.2:c.926+365T= (TGFB3)	ENSP00000502685.1:n.926+365T=
ENST00000238682.7:c.926+365T= (TGFB3)	ENSP00000238682.3:n.926+365T=
ENST00000554980.5:n.1307+365T= (TGFB3)
ENST00000555677.5:n.90-25934A= (IFT43)
ENST00000557493.1:n.392+365T= (TGFB3)
NM_003239.3:c.926+365T= (TGFB3)	NP_003230.1:n.926+365T=
XM_005268028.1:c.926+365T= (TGFB3)	XP_005268085.1:n.926+365T=
NM_001329939.1:c.926+365T= (TGFB3)	NP_001316868.1:n.926+365T=
NM_003239.4:c.926+365T= (TGFB3)	NP_003230.1:n.926+365T=
NM_001329939.2:c.926+365T= (TGFB3)	NP_001316868.1:n.926+365T=
NM_003239.5:c.926+365T= (TGFB3) MANE Select	NP_003230.1:n.926+365T=