Canonical Allele Identifier: CA2625771774

Gene: TGFB3 IFT43

Linked Data

• gnomAD v4: 14-75963276-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75963276C>T , CM000676.2:g.75963276C>T	GRCh38
NC_000014.8:g.76429619C>T , CM000676.1:g.76429619C>T	GRCh37
NC_000014.7:g.75499372C>T	NCBI36
NG_011715.1:g.23474G>A , LRG_399:g.23474G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000238682.8:c.926+40G>A (TGFB3) MANE Select	ENSP00000238682.3:n.926+40G>A
ENST00000556674.2:c.926+40G>A (TGFB3)	ENSP00000502685.1:n.926+40G>A
ENST00000238682.7:c.926+40G>A (TGFB3)	ENSP00000238682.3:n.926+40G>A
ENST00000554980.5:n.1307+40G>A (TGFB3)
ENST00000555677.5:n.90-25609C>T (IFT43)
ENST00000556285.1:c.*36G>A (TGFB3)	ENSP00000451110.1:n.*36G>A
ENST00000557493.1:n.392+40G>A (TGFB3)
NM_003239.3:c.926+40G>A (TGFB3)	NP_003230.1:n.926+40G>A
XM_005268028.1:c.926+40G>A (TGFB3)	XP_005268085.1:n.926+40G>A
NM_001329938.1:c.*36G>A (TGFB3)	NP_001316867.1:n.*36G>A
NM_001329939.1:c.926+40G>A (TGFB3)	NP_001316868.1:n.926+40G>A
NM_003239.4:c.926+40G>A (TGFB3)	NP_003230.1:n.926+40G>A
NM_001329938.2:c.*36G>A (TGFB3)	NP_001316867.1:n.*36G>A
NM_001329939.2:c.926+40G>A (TGFB3)	NP_001316868.1:n.926+40G>A
NM_003239.5:c.926+40G>A (TGFB3) MANE Select	NP_003230.1:n.926+40G>A