Canonical Allele Identifier: CA2147720446

Linked Data

dbSNP Id: rs2035177437

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75963140_75963141insT , CM000676.2:g.75963140_75963141insT GRCh38
NC_000014.8:g.76429483_76429484insT , CM000676.1:g.76429483_76429484insT GRCh37
NC_000014.7:g.75499236_75499237insT NCBI36
NG_011715.1:g.23609_23610insA , LRG_399:g.23609_23610insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000238682.8:c.926+175_926+176insA (TGFB3) MANE Select ENSP00000238682.3:n.926+175_926+176insA
ENST00000556674.2:c.926+175_926+176insA (TGFB3) ENSP00000502685.1:n.926+175_926+176insA
ENST00000238682.7:c.926+175_926+176insA (TGFB3) ENSP00000238682.3:n.926+175_926+176insA
ENST00000554980.5:n.1307+175_1307+176insA (TGFB3)
ENST00000555677.5:n.90-25745_90-25744insT (IFT43)
ENST00000556285.1:c.*171_*172insA (TGFB3) ENSP00000451110.1:n.*171_*172insA
ENST00000557493.1:n.392+175_392+176insA (TGFB3)
NM_003239.3:c.926+175_926+176insA (TGFB3) NP_003230.1:n.926+175_926+176insA
XM_005268028.1:c.926+175_926+176insA (TGFB3) XP_005268085.1:n.926+175_926+176insA
NM_001329938.1:c.*171_*172insA (TGFB3) NP_001316867.1:n.*171_*172insA
NM_001329939.1:c.926+175_926+176insA (TGFB3) NP_001316868.1:n.926+175_926+176insA
NM_003239.4:c.926+175_926+176insA (TGFB3) NP_003230.1:n.926+175_926+176insA
NM_001329938.2:c.*171_*172insA (TGFB3) NP_001316867.1:n.*171_*172insA
NM_001329939.2:c.926+175_926+176insA (TGFB3) NP_001316868.1:n.926+175_926+176insA
NM_003239.5:c.926+175_926+176insA (TGFB3) MANE Select NP_003230.1:n.926+175_926+176insA