Canonical Allele Identifier: CA2839987450

Gene: TFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633146dup , CM000669.2:g.100633146dup	GRCh38
NC_000007.13:g.100230769dup , CM000669.1:g.100230769dup	GRCh37
NC_000007.12:g.100068705dup	NCBI36
NG_007989.1:g.13406dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.727-22dup MANE Select	ENSP00000223051.3:n.727-22dup
ENST00000223051.7:c.727-22dup	ENSP00000223051.3:n.727-22dup
ENST00000431692.5:c.727-22dup	ENSP00000413905.1:n.727-22dup
ENST00000462107.1:c.727-22dup	ENSP00000420525.1:n.727-22dup
ENST00000465294.5:n.732-22dup
ENST00000473374.5:n.177-22dup
ENST00000473571.1:n.181-22dup
ENST00000475011.1:n.256-22dup
ENST00000476304.5:n.348-22dup
NM_001206855.1:c.214-22dup	NP_001193784.1:n.214-22dup
NM_003227.3:c.727-22dup	NP_003218.2:n.727-22dup
XM_005250553.3:c.727-22dup	XP_005250610.1:n.727-22dup
XM_005250554.3:c.727-22dup	XP_005250611.1:n.727-22dup
NM_001206855.2:c.214-22dup	NP_001193784.1:n.214-22dup
XM_005250553.4:c.727-22dup	XP_005250610.1:n.727-22dup
XM_017012573.1:c.727-22dup	XP_016868062.1:n.727-22dup
NM_003227.4:c.727-22dup MANE Select	NP_003218.2:n.727-22dup
NM_001206855.3:c.214-22dup	NP_001193784.1:n.214-22dup