Canonical Allele Identifier: CA2744558633
Gene: TGFBR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.91866851_91866855del , CM000663.2:g.91866851_91866855del GRCh38
NC_000001.10:g.92332408_92332412del , CM000663.1:g.92332408_92332412del GRCh37
NC_000001.9:g.92104996_92105000del NCBI36
NG_027757.1:g.44149_44153del

Transcript Alleles

HGVS Amino-acid Change
ENST00000212355.9:c.-113-5210_-113-5206del MANE Select ENSP00000212355.4:n.-113-5210_-113-5206del
ENST00000212355.8:c.-113-5210_-113-5206del ENSP00000212355.4:n.-113-5210_-113-5206del
ENST00000370399.6:c.-113-5210_-113-5206del ENSP00000359426.2:n.-113-5210_-113-5206del
ENST00000417833.2:c.-200-12_-200-8del ENSP00000395975.2:n.-200-12_-200-8del
ENST00000465892.6:c.-113-5210_-113-5206del ENSP00000432638.1:n.-113-5210_-113-5206del
ENST00000532540.5:c.-113-5210_-113-5206del ENSP00000434994.1:n.-113-5210_-113-5206del
ENST00000533370.1:n.123-2575_123-2571del
NM_001195683.1:c.-113-5210_-113-5206del NP_001182612.1:n.-113-5210_-113-5206del
NM_001195684.1:c.-113-5210_-113-5206del NP_001182613.1:n.-113-5210_-113-5206del
NM_003243.4:c.-113-5210_-113-5206del NP_003234.2:n.-113-5210_-113-5206del
NR_036634.1:n.403-5210_403-5206del
XM_006710867.1:c.-113-5210_-113-5206del XP_006710930.1:n.-113-5210_-113-5206del
XM_006710867.2:c.-113-5210_-113-5206del XP_006710930.1:n.-113-5210_-113-5206del
NM_003243.5:c.-113-5210_-113-5206del MANE Select NP_003234.2:n.-113-5210_-113-5206del
NM_001195683.2:c.-113-5210_-113-5206del NP_001182612.1:n.-113-5210_-113-5206del
NR_036634.2:n.275-5210_275-5206del