Canonical Allele Identifier: CA2840494229

Gene: TFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100632960dup , CM000669.2:g.100632960dup	GRCh38
NC_000007.13:g.100230583dup , CM000669.1:g.100230583dup	GRCh37
NC_000007.12:g.100068519dup	NCBI36
NG_007989.1:g.13592dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.849+42dup MANE Select	ENSP00000223051.3:n.849+42dup
ENST00000223051.7:c.849+42dup	ENSP00000223051.3:n.849+42dup
ENST00000431692.5:c.849+42dup	ENSP00000413905.1:n.849+42dup
ENST00000462090.5:n.90+42dup
ENST00000462107.1:c.849+42dup	ENSP00000420525.1:n.849+42dup
ENST00000465294.5:n.854+42dup
ENST00000473374.5:n.299+42dup
ENST00000473571.1:n.303+42dup
ENST00000475011.1:n.420dup
ENST00000476304.5:n.470+42dup
ENST00000490084.5:c.104+42dup
NM_001206855.1:c.336+42dup	NP_001193784.1:n.336+42dup
NM_003227.3:c.849+42dup	NP_003218.2:n.849+42dup
XM_005250553.3:c.849+42dup	XP_005250610.1:n.849+42dup
XM_005250554.3:c.849+42dup	XP_005250611.1:n.849+42dup
XR_927814.1:n.541dup
NM_001206855.2:c.336+42dup	NP_001193784.1:n.336+42dup
XM_005250553.4:c.849+42dup	XP_005250610.1:n.849+42dup
XM_017012573.1:c.849+42dup	XP_016868062.1:n.849+42dup
NM_003227.4:c.849+42dup MANE Select	NP_003218.2:n.849+42dup
NM_001206855.3:c.336+42dup	NP_001193784.1:n.336+42dup