Canonical Allele Identifier: CA2585296380

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342126-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342132_41342133del , CM000681.2:g.41342132_41342133del	GRCh38
NC_000019.9:g.41848037_41848038del , CM000681.1:g.41848037_41848038del	GRCh37
NC_000019.8:g.46539877_46539878del	NCBI36
NG_013364.1:g.16799_16800del

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.712+42_712+43del MANE Select	ENSP00000221930.4:n.712+42_712+43del
ENST00000600196.2:c.712+42_712+43del	ENSP00000504008.1:n.712+42_712+43del
ENST00000677934.1:c.634+2619_634+2620del	ENSP00000504769.1:n.634+2619_634+2620del
ENST00000221930.5:c.712+42_712+43del	ENSP00000221930.4:n.712+42_712+43del
ENST00000597453.1:n.285_286del
ENST00000600196.1:n.172+42_172+43del
NM_000660.5:c.712+42_712+43del	NP_000651.3:n.712+42_712+43del
XM_011527242.1:c.712+42_712+43del	XP_011525544.1:n.712+42_712+43del
NM_000660.6:c.712+42_712+43del	NP_000651.3:n.712+42_712+43del
XM_011527242.2:c.712+42_712+43del	XP_011525544.1:n.712+42_712+43del
NM_000660.7:c.712+42_712+43del MANE Select	NP_000651.3:n.712+42_712+43del