Canonical Allele Identifier: CA2336421077

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342115_41342119delinsAACAC , CM000681.2:g.41342115_41342119delinsAACAC	GRCh38
NC_000019.9:g.41848020_41848024delinsAACAC , CM000681.1:g.41848020_41848024delinsAACAC	GRCh37
NC_000019.8:g.46539860_46539864delinsAACAC	NCBI36
NG_013364.1:g.16808_16812delinsGTGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.712+51_712+55delinsGTGTT MANE Select	ENSP00000221930.4:n.712+51_712+55delinsGT...
ENST00000600196.2:c.712+51_712+55delinsGTGTT	ENSP00000504008.1:n.712+51_712+55delinsGT...
ENST00000677934.1:c.634+2628_634+2632delinsGTGTT	ENSP00000504769.1:n.634+2628_634+2632deli...
ENST00000221930.5:c.712+51_712+55delinsGTGTT	ENSP00000221930.4:n.712+51_712+55delinsGT...
ENST00000597453.1:n.294_298delinsGTGTT
ENST00000600196.1:n.172+51_172+55delinsGTGTT
NM_000660.5:c.712+51_712+55delinsGTGTT	NP_000651.3:n.712+51_712+55delinsGTGTT
XM_011527242.1:c.712+51_712+55delinsGTGTT	XP_011525544.1:n.712+51_712+55delinsGTGTT...
NM_000660.6:c.712+51_712+55delinsGTGTT	NP_000651.3:n.712+51_712+55delinsGTGTT
XM_011527242.2:c.712+51_712+55delinsGTGTT	XP_011525544.1:n.712+51_712+55delinsGTGTT...
NM_000660.7:c.712+51_712+55delinsGTGTT MANE Select	NP_000651.3:n.712+51_712+55delinsGTGTT