Canonical Allele Identifier: CA2336416577

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332473_41332474delinsTC , CM000681.2:g.41332473_41332474delinsTC	GRCh38
NC_000019.9:g.41838378_41838379delinsTC , CM000681.1:g.41838378_41838379delinsTC	GRCh37
NC_000019.8:g.46530218_46530219delinsTC	NCBI36
NG_013364.1:g.26453_26454delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-193_861-192delinsGA MANE Select	ENSP00000221930.4:n.861-193_861-192delinsGA
ENST00000600196.2:c.713-193_713-192delinsGA	ENSP00000504008.1:n.713-193_713-192delinsGA
ENST00000677934.1:c.635-193_635-192delinsGA	ENSP00000504769.1:n.635-193_635-192delinsGA
ENST00000221930.5:c.861-193_861-192delinsGA	ENSP00000221930.4:n.861-193_861-192delinsGA
ENST00000598758.5:c.149-193_149-192delinsGA
ENST00000600196.1:n.173-193_173-192delinsGA
NM_000660.5:c.861-193_861-192delinsGA	NP_000651.3:n.861-193_861-192delinsGA
XM_011527242.1:c.864-193_864-192delinsGA	XP_011525544.1:n.864-193_864-192delinsGA
NM_000660.6:c.861-193_861-192delinsGA	NP_000651.3:n.861-193_861-192delinsGA
XM_011527242.2:c.864-193_864-192delinsGA	XP_011525544.1:n.864-193_864-192delinsGA
NM_000660.7:c.861-193_861-192delinsGA MANE Select	NP_000651.3:n.861-193_861-192delinsGA