Canonical Allele Identifier: CA2814427360

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332394_41332395insAAA , CM000681.2:g.41332394_41332395insAAA	GRCh38
NC_000019.9:g.41838299_41838300insAAA , CM000681.1:g.41838299_41838300insAAA	GRCh37
NC_000019.8:g.46530139_46530140insAAA	NCBI36
NG_013364.1:g.26532_26533insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-114_861-113insTTT MANE Select	ENSP00000221930.4:n.861-114_861-113insTTT
ENST00000600196.2:c.713-114_713-113insTTT	ENSP00000504008.1:n.713-114_713-113insTTT
ENST00000677934.1:c.635-114_635-113insTTT	ENSP00000504769.1:n.635-114_635-113insTTT
ENST00000221930.5:c.861-114_861-113insTTT	ENSP00000221930.4:n.861-114_861-113insTTT
ENST00000598758.5:c.149-114_149-113insTTT
ENST00000600196.1:n.173-114_173-113insTTT
NM_000660.5:c.861-114_861-113insTTT	NP_000651.3:n.861-114_861-113insTTT
XM_011527242.1:c.864-114_864-113insTTT	XP_011525544.1:n.864-114_864-113insTTT
NM_000660.6:c.861-114_861-113insTTT	NP_000651.3:n.861-114_861-113insTTT
XM_011527242.2:c.864-114_864-113insTTT	XP_011525544.1:n.864-114_864-113insTTT
NM_000660.7:c.861-114_861-113insTTT MANE Select	NP_000651.3:n.861-114_861-113insTTT