Canonical Allele Identifier: CA368526167

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100225283T>A (hg19) ; chr7:g.100627660T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100627660T>A , CM000669.2:g.100627660T>A	GRCh38
NC_000007.13:g.100225283T>A , CM000669.1:g.100225283T>A	GRCh37
NC_000007.12:g.100063219T>A	NCBI36
NG_007989.1:g.18891A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.1684A>T MANE Select	ENSP00000223051.3:p.Ile562Phe
ENST00000223051.7:c.1684A>T	ENSP00000223051.3:p.Ile562Phe
ENST00000431692.5:c.*359A>T	ENSP00000413905.1:n.*359A>T
ENST00000462090.5:n.635A>T
ENST00000462107.1:c.1684A>T	ENSP00000420525.1:p.Ile562Phe
ENST00000465294.5:n.1519A>T
ENST00000473374.5:n.757A>T
ENST00000473963.1:n.713A>T
ENST00000476304.5:n.1305A>T
ENST00000490084.5:c.1037A>T
NM_001206855.1:c.1171A>T	NP_001193784.1:p.Ile391Phe
NM_003227.3:c.1684A>T	NP_003218.2:p.Ile562Phe
XM_005250553.3:c.1684A>T	XP_005250610.1:p.Ile562Phe
XM_005250554.3:c.1684A>T	XP_005250611.1:p.Ile562Phe
XR_927814.1:n.434-3496T>A
NM_001206855.2:c.1171A>T	NP_001193784.1:p.Ile391Phe
XM_005250553.4:c.1684A>T	XP_005250610.1:p.Ile562Phe
XM_017012573.1:c.1684A>T	XP_016868062.1:p.Ile562Phe
NM_003227.4:c.1684A>T MANE Select	NP_003218.2:p.Ile562Phe
NM_001206855.3:c.1171A>T	NP_001193784.1:p.Ile391Phe