Canonical Allele Identifier: CA1143401123

Gene: TGFB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.218346650_218346657delinsTTTTTTTT , CM000663.2:g.218346650_218346657delinsTTTTTTTT	GRCh38
NC_000001.10:g.218519992_218519999delinsTTTTTTTT , CM000663.1:g.218519992_218519999delinsTTTTTTTT	GRCh37
NC_000001.9:g.216586615_216586622delinsTTTTTTTT	NCBI36
NG_027721.1:g.6317_6324delinsTTTTTTTT
NG_027721.2:g.6317_6324delinsTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366930.9:c.-52_-45delinsTTTTTTTT MANE Select	ENSP00000355897.4:n.-52_-45delinsTTTTTTTT
ENST00000366929.4:c.-52_-45delinsTTTTTTTT	ENSP00000355896.4:n.-52_-45delinsTTTTTTTT
ENST00000366930.8:c.-52_-45delinsTTTTTTTT	ENSP00000355897.4:n.-52_-45delinsTTTTTTTT
NM_001135599.2:c.-52_-45delinsTTTTTTTT	NP_001129071.1:n.-52_-45delinsTTTTTTTT
NM_003238.3:c.-52_-45delinsTTTTTTTT	NP_003229.1:n.-52_-45delinsTTTTTTTT
NM_001135599.3:c.-52_-45delinsTTTTTTTT	NP_001129071.1:n.-52_-45delinsTTTTTTTT
NM_003238.4:c.-52_-45delinsTTTTTTTT	NP_003229.1:n.-52_-45delinsTTTTTTTT
NR_138148.1:n.1367_1374delinsTTTTTTTT
NR_138149.1:n.1367_1374delinsTTTTTTTT
NM_003238.5:c.-52_-45delinsTTTTTTTT	NP_003229.1:n.-52_-45delinsTTTTTTTT
NM_003238.6:c.-52_-45delinsTTTTTTTT MANE Select	NP_003229.1:n.-52_-45delinsTTTTTTTT
NM_001135599.4:c.-52_-45delinsTTTTTTTT	NP_001129071.1:n.-52_-45delinsTTTTTTTT
NR_138148.2:n.1315_1322delinsTTTTTTTT
NR_138149.2:n.1315_1322delinsTTTTTTTT