Canonical Allele Identifier: CA2336416555

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332412_41332413delinsCA , CM000681.2:g.41332412_41332413delinsCA	GRCh38
NC_000019.9:g.41838317_41838318delinsCA , CM000681.1:g.41838317_41838318delinsCA	GRCh37
NC_000019.8:g.46530157_46530158delinsCA	NCBI36
NG_013364.1:g.26514_26515delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-132_861-131delinsTG MANE Select	ENSP00000221930.4:n.861-132_861-131delinsTG
ENST00000600196.2:c.713-132_713-131delinsTG	ENSP00000504008.1:n.713-132_713-131delinsTG
ENST00000677934.1:c.635-132_635-131delinsTG	ENSP00000504769.1:n.635-132_635-131delinsTG
ENST00000221930.5:c.861-132_861-131delinsTG	ENSP00000221930.4:n.861-132_861-131delinsTG
ENST00000598758.5:c.149-132_149-131delinsTG
ENST00000600196.1:n.173-132_173-131delinsTG
NM_000660.5:c.861-132_861-131delinsTG	NP_000651.3:n.861-132_861-131delinsTG
XM_011527242.1:c.864-132_864-131delinsTG	XP_011525544.1:n.864-132_864-131delinsTG
NM_000660.6:c.861-132_861-131delinsTG	NP_000651.3:n.861-132_861-131delinsTG
XM_011527242.2:c.864-132_864-131delinsTG	XP_011525544.1:n.864-132_864-131delinsTG
NM_000660.7:c.861-132_861-131delinsTG MANE Select	NP_000651.3:n.861-132_861-131delinsTG