Canonical Allele Identifier: CA2336421220

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342388_41342392delinsCTCTT , CM000681.2:g.41342388_41342392delinsCTCTT	GRCh38
NC_000019.9:g.41848293_41848297delinsCTCTT , CM000681.1:g.41848293_41848297delinsCTCTT	GRCh37
NC_000019.8:g.46540133_46540137delinsCTCTT	NCBI36
NG_013364.1:g.16535_16539delinsAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-145_635-141delinsAAGAG MANE Select	ENSP00000221930.4:n.635-145_635-141delinsAAGAG
ENST00000600196.2:c.635-145_635-141delinsAAGAG	ENSP00000504008.1:n.635-145_635-141delinsAAGAG
ENST00000677934.1:c.634+2355_634+2359delinsAAGAG	ENSP00000504769.1:n.634+2355_634+2359delinsAAGAG
ENST00000221930.5:c.635-145_635-141delinsAAGAG	ENSP00000221930.4:n.635-145_635-141delinsAAGAG
ENST00000597453.1:n.166-145_166-141delinsAAGAG
ENST00000600196.1:n.95-145_95-141delinsAAGAG
NM_000660.5:c.635-145_635-141delinsAAGAG	NP_000651.3:n.635-145_635-141delinsAAGAG
XM_011527242.1:c.635-145_635-141delinsAAGAG	XP_011525544.1:n.635-145_635-141delinsAAGAG
NM_000660.6:c.635-145_635-141delinsAAGAG	NP_000651.3:n.635-145_635-141delinsAAGAG
XM_011527242.2:c.635-145_635-141delinsAAGAG	XP_011525544.1:n.635-145_635-141delinsAAGAG
NM_000660.7:c.635-145_635-141delinsAAGAG MANE Select	NP_000651.3:n.635-145_635-141delinsAAGAG