Canonical Allele Identifier: CA2336421225
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342390_41342405delinsCTTTTTTTTTTTTTTT , CM000681.2:g.41342390_41342405delinsCTTTTTTTTTTTTTTT GRCh38
NC_000019.9:g.41848295_41848310delinsCTTTTTTTTTTTTTTT , CM000681.1:g.41848295_41848310delinsCTTTTTTTTTTTTTTT GRCh37
NC_000019.8:g.46540135_46540150delinsCTTTTTTTTTTTTTTT NCBI36
NG_013364.1:g.16522_16537delinsAAAAAAAAAAAAAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-158_635-143delinsAAAAAAAAAAAAAAAG MANE Select ENSP00000221930.4:n.635-158_635-143delinsAAAAAAAAAAAAAAAG
ENST00000600196.2:c.635-158_635-143delinsAAAAAAAAAAAAAAAG ENSP00000504008.1:n.635-158_635-143delinsAAAAAAAAAAAAAAAG
ENST00000677934.1:c.634+2342_634+2357delinsAAAAAAAAAAAAAAAG ENSP00000504769.1:n.634+2342_634+2357delinsAAAAAAAAAAAAAAAG
ENST00000221930.5:c.635-158_635-143delinsAAAAAAAAAAAAAAAG ENSP00000221930.4:n.635-158_635-143delinsAAAAAAAAAAAAAAAG
ENST00000597453.1:n.166-158_166-143delinsAAAAAAAAAAAAAAAG
ENST00000600196.1:n.95-158_95-143delinsAAAAAAAAAAAAAAAG
NM_000660.5:c.635-158_635-143delinsAAAAAAAAAAAAAAAG NP_000651.3:n.635-158_635-143delinsAAAAAAAAAAAAAAAG
XM_011527242.1:c.635-158_635-143delinsAAAAAAAAAAAAAAAG XP_011525544.1:n.635-158_635-143delinsAAAAAAAAAAAAAAAG
NM_000660.6:c.635-158_635-143delinsAAAAAAAAAAAAAAAG NP_000651.3:n.635-158_635-143delinsAAAAAAAAAAAAAAAG
XM_011527242.2:c.635-158_635-143delinsAAAAAAAAAAAAAAAG XP_011525544.1:n.635-158_635-143delinsAAAAAAAAAAAAAAAG
NM_000660.7:c.635-158_635-143delinsAAAAAAAAAAAAAAAG MANE Select NP_000651.3:n.635-158_635-143delinsAAAAAAAAAAAAAAAG