Canonical Allele Identifier: CA2147725144

Gene: TGFB3 IFT43

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75971629G= , CM000676.2:g.75971629G=	GRCh38
NC_000014.8:g.76437972G= , CM000676.1:g.76437972G=	GRCh37
NC_000014.7:g.75507725G=	NCBI36
NG_011715.1:g.15121C= , LRG_399:g.15121C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003239.5:c.442C= (TGFB3) MANE Select	NP_003230.1:p.Arg148=
ENST00000238682.8:c.442C= (TGFB3) MANE Select	ENSP00000238682.3:p.Arg148=
NM_001329938.1:c.442C= (TGFB3)	NP_001316867.1:p.Arg148=
NM_001329938.2:c.442C= (TGFB3)	NP_001316867.1:p.Arg148=
NM_001329939.1:c.442C= (TGFB3)	NP_001316868.1:p.Arg148=
NM_001329939.2:c.442C= (TGFB3)	NP_001316868.1:p.Arg148=
NM_003239.3:c.442C= (TGFB3)	NP_003230.1:p.Arg148=
NM_003239.4:c.442C= (TGFB3)	NP_003230.1:p.Arg148=
ENST00000238682.7:c.442C= (TGFB3)	ENSP00000238682.3:p.Arg148=
ENST00000555677.5:n.90-17256G= (IFT43)
ENST00000556285.1:c.442C= (TGFB3)	ENSP00000451110.1:p.Arg148=
ENST00000556674.2:c.442C= (TGFB3)	ENSP00000502685.1:p.Arg148=
XM_005268028.1:c.442C= (TGFB3)	XP_005268085.1:p.Arg148=