Canonical Allele Identifier: CA2585296721

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41348143-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348143_41348144insGG , CM000681.2:g.41348143_41348144insGG	GRCh38
NC_000019.9:g.41854048_41854049insGG , CM000681.1:g.41854048_41854049insGG	GRCh37
NC_000019.8:g.46545888_46545889insGG	NCBI36
NG_013364.1:g.10783_10784insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.516+151_516+152insCC MANE Select	ENSP00000221930.4:n.516+151_516+152insCC
ENST00000600196.2:c.516+151_516+152insCC	ENSP00000504008.1:n.516+151_516+152insCC
ENST00000677934.1:c.516+151_516+152insCC	ENSP00000504769.1:n.516+151_516+152insCC
ENST00000221930.5:c.516+151_516+152insCC	ENSP00000221930.4:n.516+151_516+152insCC
ENST00000597453.1:n.47+151_47+152insCC
NM_000660.5:c.516+151_516+152insCC	NP_000651.3:n.516+151_516+152insCC
XM_011527242.1:c.516+151_516+152insCC	XP_011525544.1:n.516+151_516+152insCC
NM_000660.6:c.516+151_516+152insCC	NP_000651.3:n.516+151_516+152insCC
XM_011527242.2:c.516+151_516+152insCC	XP_011525544.1:n.516+151_516+152insCC
NM_000660.7:c.516+151_516+152insCC MANE Select	NP_000651.3:n.516+151_516+152insCC