Canonical Allele Identifier: CA2740686285
Gene: TGFBI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.136056739_136056740insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT , CM000667.2:g.136056739_136056740insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT GRCh38
NC_000005.9:g.135392428_135392429insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT , CM000667.1:g.135392428_135392429insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT GRCh37
NC_000005.8:g.135420327_135420328insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT NCBI36
NG_012646.1:g.32845_32846insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000442011.7:c.1622_1623insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT MANE Select ENSP00000416330.2:p.Ala542GlyfsTer11
ENST00000442011.6:c.1622_1623insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT ENSP00000416330.2:p.Ala542GlyfsTer11
ENST00000506699.5:n.2139_2140insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT
ENST00000507018.5:c.1600_1601insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT
ENST00000509485.5:c.619_620insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT
ENST00000514242.5:n.393_394insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT
ENST00000514554.5:c.774_775insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT
NM_000358.2:c.1622_1623insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT NP_000349.1:p.Ala542GlyfsTer11
NM_000358.3:c.1622_1623insCGGCCTCGATTATTGTGAAGCGTTACCGCCGTAAGGATTCGACGGTGAACGCGGGCGGTTTCGGGTACCTGCGTGAGCGCTACGGTTTGGAGGCGCTGAACCGGCAGGTTCCGGGTCTGT MANE Select NP_000349.1:p.Ala542GlyfsTer11