Canonical Allele Identifier: CA1917456291

Gene: TET1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68692714C>G , CM000672.2:g.68692714C>G	GRCh38
NC_000010.10:g.70452471C>G , CM000672.1:g.70452471C>G	GRCh37
NC_000010.9:g.70122477C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373644.5:c.*900C>G MANE Select	ENSP00000362748.4:n.*900C>G
ENST00000373644.4:c.*900C>G	ENSP00000362748.4:n.*900C>G
NM_030625.2:c.*900C>G	NP_085128.2:n.*900C>G
XM_011540204.1:c.*900C>G	XP_011538506.1:n.*900C>G
XM_011540205.1:c.*900C>G	XP_011538507.1:n.*900C>G
XM_011540207.1:c.*900C>G	XP_011538509.1:n.*900C>G
XM_011540204.2:c.*900C>G	XP_011538506.1:n.*900C>G
XM_011540205.2:c.*900C>G	XP_011538507.1:n.*900C>G
XM_011540207.2:c.*900C>G	XP_011538509.1:n.*900C>G
XM_017016686.2:c.*900C>G	XP_016872175.1:n.*900C>G
XM_017016687.1:c.*900C>G	XP_016872176.1:n.*900C>G
XM_017016688.1:c.*900C>G	XP_016872177.1:n.*900C>G
XM_017016689.1:c.*900C>G	XP_016872178.1:n.*900C>G
NM_030625.3:c.*900C>G MANE Select	NP_085128.2:n.*900C>G