Canonical Allele Identifier: CA1140581375
Gene: TGFBR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.91705226_91705242delinsTTTTTTTTTTTTTTTTT , CM000663.2:g.91705226_91705242delinsTTTTTTTTTTTTTTTTT GRCh38
NC_000001.10:g.92170783_92170799delinsTTTTTTTTTTTTTTTTT , CM000663.1:g.92170783_92170799delinsTTTTTTTTTTTTTTTTT GRCh37
NC_000001.9:g.91943371_91943387delinsTTTTTTTTTTTTTTTTT NCBI36
NG_027757.1:g.205761_205777delinsAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000212355.9:c.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA MANE Select ENSP00000212355.4:n.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAA...
ENST00000212355.8:c.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA ENSP00000212355.4:n.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAA...
ENST00000370399.6:c.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAAA ENSP00000359426.2:n.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAA...
ENST00000465892.6:c.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAAA ENSP00000432638.1:n.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAA...
ENST00000470600.1:n.242+3421_242+3437delinsAAAAAAAAAAAAAAAAA
ENST00000525962.5:c.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA ENSP00000436127.1:n.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAA...
ENST00000532540.5:c.*2234+3421_*2234+3437delinsAAAAAAAAAAAAAAAAA ENSP00000434994.1:n.*2234+3421_*2234+3437delinsAAAAAAAAAAAAAA...
ENST00000533089.5:c.*2005+3421_*2005+3437delinsAAAAAAAAAAAAAAAAA ENSP00000433477.1:n.*2005+3421_*2005+3437delinsAAAAAAAAAAAAAA...
NM_001195683.1:c.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAAA NP_001182612.1:n.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAAA
NM_001195684.1:c.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAAA NP_001182613.1:n.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAAA
NM_003243.4:c.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA NP_003234.2:n.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA
NR_036634.1:n.2899+3421_2899+3437delinsAAAAAAAAAAAAAAAAA
XM_006710867.1:c.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA XP_006710930.1:n.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA
XM_006710868.1:c.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA XP_006710931.1:n.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA
XM_011542058.1:c.1621+3421_1621+3437delinsAAAAAAAAAAAAAAAAA XP_011540360.1:n.1621+3421_1621+3437delinsAAAAAAAAAAAAAAAAA
XM_006710867.2:c.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA XP_006710930.1:n.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA
NM_003243.5:c.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA MANE Select NP_003234.2:n.2287+3421_2287+3437delinsAAAAAAAAAAAAAAAAA
NM_001195683.2:c.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAAA NP_001182612.1:n.2284+3421_2284+3437delinsAAAAAAAAAAAAAAAAA
NR_036634.2:n.2771+3421_2771+3437delinsAAAAAAAAAAAAAAAAA