Canonical Allele Identifier: CA2814427067

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342359_41342360insAACACA , CM000681.2:g.41342359_41342360insAACACA	GRCh38
NC_000019.9:g.41848264_41848265insAACACA , CM000681.1:g.41848264_41848265insAACACA	GRCh37
NC_000019.8:g.46540104_46540105insAACACA	NCBI36
NG_013364.1:g.16569_16570insTGTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-111_635-110insTGTTTG MANE Select	ENSP00000221930.4:n.635-111_635-110insTGTTTG
ENST00000600196.2:c.635-111_635-110insTGTTTG	ENSP00000504008.1:n.635-111_635-110insTGTTTG
ENST00000677934.1:c.634+2389_634+2390insTGTTTG	ENSP00000504769.1:n.634+2389_634+2390insTGTTTG
ENST00000221930.5:c.635-111_635-110insTGTTTG	ENSP00000221930.4:n.635-111_635-110insTGTTTG
ENST00000597453.1:n.166-111_166-110insTGTTTG
ENST00000600196.1:n.95-111_95-110insTGTTTG
NM_000660.5:c.635-111_635-110insTGTTTG	NP_000651.3:n.635-111_635-110insTGTTTG
XM_011527242.1:c.635-111_635-110insTGTTTG	XP_011525544.1:n.635-111_635-110insTGTTTG
NM_000660.6:c.635-111_635-110insTGTTTG	NP_000651.3:n.635-111_635-110insTGTTTG
XM_011527242.2:c.635-111_635-110insTGTTTG	XP_011525544.1:n.635-111_635-110insTGTTTG
NM_000660.7:c.635-111_635-110insTGTTTG MANE Select	NP_000651.3:n.635-111_635-110insTGTTTG