Canonical Allele Identifier: CA2147720578

Gene: TGFB3 IFT43

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75963277A= , CM000676.2:g.75963277A=	GRCh38
NC_000014.8:g.76429620A= , CM000676.1:g.76429620A=	GRCh37
NC_000014.7:g.75499373A=	NCBI36
NG_011715.1:g.23473T= , LRG_399:g.23473T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000238682.8:c.926+39T= (TGFB3) MANE Select	ENSP00000238682.3:n.926+39T=
ENST00000556674.2:c.926+39T= (TGFB3)	ENSP00000502685.1:n.926+39T=
ENST00000238682.7:c.926+39T= (TGFB3)	ENSP00000238682.3:n.926+39T=
ENST00000554980.5:n.1307+39T= (TGFB3)
ENST00000555677.5:n.90-25608A= (IFT43)
ENST00000556285.1:c.*35T= (TGFB3)	ENSP00000451110.1:n.*35T=
ENST00000557493.1:n.392+39T= (TGFB3)
NM_003239.3:c.926+39T= (TGFB3)	NP_003230.1:n.926+39T=
XM_005268028.1:c.926+39T= (TGFB3)	XP_005268085.1:n.926+39T=
NM_001329938.1:c.*35T= (TGFB3)	NP_001316867.1:n.*35T=
NM_001329939.1:c.926+39T= (TGFB3)	NP_001316868.1:n.926+39T=
NM_003239.4:c.926+39T= (TGFB3)	NP_003230.1:n.926+39T=
NM_001329938.2:c.*35T= (TGFB3)	NP_001316867.1:n.*35T=
NM_001329939.2:c.926+39T= (TGFB3)	NP_001316868.1:n.926+39T=
NM_003239.5:c.926+39T= (TGFB3) MANE Select	NP_003230.1:n.926+39T=