Canonical Allele Identifier: CA1917456292

Gene: TET1

Genomic Alleles

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

Transcript Alleles

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