Canonical Allele Identifier: CA2147722491

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75965501G= , CM000676.2:g.75965501G= GRCh38
NC_000014.8:g.76431844G= , CM000676.1:g.76431844G= GRCh37
NC_000014.7:g.75501597G= NCBI36
NG_011715.1:g.21249C= , LRG_399:g.21249C=

Transcript Alleles

HGVS Amino-acid change
ENST00000238682.8:c.754+87C= (TGFB3) MANE Select ENSP00000238682.3:n.754+87C=
ENST00000556674.2:c.754+87C= (TGFB3) ENSP00000502685.1:n.754+87C=
ENST00000238682.7:c.754+87C= (TGFB3) ENSP00000238682.3:n.754+87C=
ENST00000554980.5:n.1135+87C= (TGFB3)
ENST00000555677.5:n.90-23384G= (IFT43)
ENST00000556285.1:c.754+87C= (TGFB3) ENSP00000451110.1:n.754+87C=
ENST00000557493.1:n.220+87C= (TGFB3)
NM_003239.3:c.754+87C= (TGFB3) NP_003230.1:n.754+87C=
XM_005268028.1:c.754+87C= (TGFB3) XP_005268085.1:n.754+87C=
NM_001329938.1:c.754+87C= (TGFB3) NP_001316867.1:n.754+87C=
NM_001329939.1:c.754+87C= (TGFB3) NP_001316868.1:n.754+87C=
NM_003239.4:c.754+87C= (TGFB3) NP_003230.1:n.754+87C=
NM_001329938.2:c.754+87C= (TGFB3) NP_001316867.1:n.754+87C=
NM_001329939.2:c.754+87C= (TGFB3) NP_001316868.1:n.754+87C=
NM_003239.5:c.754+87C= (TGFB3) MANE Select NP_003230.1:n.754+87C=