Canonical Allele Identifier: CA2336421215
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342386_41342392delinsCTCTCTT , CM000681.2:g.41342386_41342392delinsCTCTCTT GRCh38
NC_000019.9:g.41848291_41848297delinsCTCTCTT , CM000681.1:g.41848291_41848297delinsCTCTCTT GRCh37
NC_000019.8:g.46540131_46540137delinsCTCTCTT NCBI36
NG_013364.1:g.16535_16541delinsAAGAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-145_635-139delinsAAGAGAG MANE Select ENSP00000221930.4:n.635-145_635-139delinsAAGAGAG
ENST00000600196.2:c.635-145_635-139delinsAAGAGAG ENSP00000504008.1:n.635-145_635-139delinsAAGAGAG
ENST00000677934.1:c.634+2355_634+2361delinsAAGAGAG ENSP00000504769.1:n.634+2355_634+2361delinsAAGAGAG
ENST00000221930.5:c.635-145_635-139delinsAAGAGAG ENSP00000221930.4:n.635-145_635-139delinsAAGAGAG
ENST00000597453.1:n.166-145_166-139delinsAAGAGAG
ENST00000600196.1:n.95-145_95-139delinsAAGAGAG
NM_000660.5:c.635-145_635-139delinsAAGAGAG NP_000651.3:n.635-145_635-139delinsAAGAGAG
XM_011527242.1:c.635-145_635-139delinsAAGAGAG XP_011525544.1:n.635-145_635-139delinsAAGAGAG
NM_000660.6:c.635-145_635-139delinsAAGAGAG NP_000651.3:n.635-145_635-139delinsAAGAGAG
XM_011527242.2:c.635-145_635-139delinsAAGAGAG XP_011525544.1:n.635-145_635-139delinsAAGAGAG
NM_000660.7:c.635-145_635-139delinsAAGAGAG MANE Select NP_000651.3:n.635-145_635-139delinsAAGAGAG