Canonical Allele Identifier: CA2336416611

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332540_41332541delinsCA , CM000681.2:g.41332540_41332541delinsCA	GRCh38
NC_000019.9:g.41838445_41838446delinsCA , CM000681.1:g.41838445_41838446delinsCA	GRCh37
NC_000019.8:g.46530285_46530286delinsCA	NCBI36
NG_013364.1:g.26386_26387delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-260_861-259delinsTG MANE Select	ENSP00000221930.4:n.861-260_861-259delinsTG
ENST00000600196.2:c.713-260_713-259delinsTG	ENSP00000504008.1:n.713-260_713-259delinsTG
ENST00000677934.1:c.635-260_635-259delinsTG	ENSP00000504769.1:n.635-260_635-259delinsTG
ENST00000221930.5:c.861-260_861-259delinsTG	ENSP00000221930.4:n.861-260_861-259delinsTG
ENST00000598758.5:c.149-260_149-259delinsTG
ENST00000600196.1:n.173-260_173-259delinsTG
NM_000660.5:c.861-260_861-259delinsTG	NP_000651.3:n.861-260_861-259delinsTG
XM_011527242.1:c.864-260_864-259delinsTG	XP_011525544.1:n.864-260_864-259delinsTG
NM_000660.6:c.861-260_861-259delinsTG	NP_000651.3:n.861-260_861-259delinsTG
XM_011527242.2:c.864-260_864-259delinsTG	XP_011525544.1:n.864-260_864-259delinsTG
NM_000660.7:c.861-260_861-259delinsTG MANE Select	NP_000651.3:n.861-260_861-259delinsTG