Canonical Allele Identifier: CA2336421036

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342037_41342038delinsTG , CM000681.2:g.41342037_41342038delinsTG	GRCh38
NC_000019.9:g.41847942_41847943delinsTG , CM000681.1:g.41847942_41847943delinsTG	GRCh37
NC_000019.8:g.46539782_46539783delinsTG	NCBI36
NG_013364.1:g.16889_16890delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.713-8_713-7delinsCA MANE Select	ENSP00000221930.4:n.713-8_713-7delinsCA
ENST00000600196.2:c.712+132_712+133delinsCA	ENSP00000504008.1:n.712+132_712+133delinsCA
ENST00000677934.1:c.634+2709_634+2710delinsCA	ENSP00000504769.1:n.634+2709_634+2710delinsCA
ENST00000221930.5:c.713-8_713-7delinsCA	ENSP00000221930.4:n.713-8_713-7delinsCA
ENST00000597453.1:n.375_376delinsCA
ENST00000600196.1:n.172+132_172+133delinsCA
NM_000660.5:c.713-8_713-7delinsCA	NP_000651.3:n.713-8_713-7delinsCA
XM_011527242.1:c.713-5_713-4delinsCA	XP_011525544.1:n.713-5_713-4delinsCA
NM_000660.6:c.713-8_713-7delinsCA	NP_000651.3:n.713-8_713-7delinsCA
XM_011527242.2:c.713-5_713-4delinsCA	XP_011525544.1:n.713-5_713-4delinsCA
NM_000660.7:c.713-8_713-7delinsCA MANE Select	NP_000651.3:n.713-8_713-7delinsCA