Canonical Allele Identifier: CA995955872

Gene: TGFB1

Linked Data

• gnomAD v3: 19-41342420-A-ATTTTTTT
• gnomAD v4: 19-41342420-A-ATTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342420_41342421insTTTTTTT , CM000681.2:g.41342420_41342421insTTTTTTT	GRCh38
NC_000019.9:g.41848325_41848326insTTTTTTT , CM000681.1:g.41848325_41848326insTTTTTTT	GRCh37
NC_000019.8:g.46540165_46540166insTTTTTTT	NCBI36
NG_013364.1:g.16506_16507insAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-174_635-173insAAAAAAA MANE Select	ENSP00000221930.4:n.635-174_635-173insAAAAAAA
ENST00000600196.2:c.635-174_635-173insAAAAAAA	ENSP00000504008.1:n.635-174_635-173insAAAAAAA
ENST00000677934.1:c.634+2326_634+2327insAAAAAAA	ENSP00000504769.1:n.634+2326_634+2327insAAAAAAA
ENST00000221930.5:c.635-174_635-173insAAAAAAA	ENSP00000221930.4:n.635-174_635-173insAAAAAAA
ENST00000597453.1:n.166-174_166-173insAAAAAAA
ENST00000600196.1:n.95-174_95-173insAAAAAAA
NM_000660.5:c.635-174_635-173insAAAAAAA	NP_000651.3:n.635-174_635-173insAAAAAAA
XM_011527242.1:c.635-174_635-173insAAAAAAA	XP_011525544.1:n.635-174_635-173insAAAAAAA
NM_000660.6:c.635-174_635-173insAAAAAAA	NP_000651.3:n.635-174_635-173insAAAAAAA
XM_011527242.2:c.635-174_635-173insAAAAAAA	XP_011525544.1:n.635-174_635-173insAAAAAAA
NM_000660.7:c.635-174_635-173insAAAAAAA MANE Select	NP_000651.3:n.635-174_635-173insAAAAAAA