Canonical Allele Identifier: CA368522887

Gene: TFR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626842T>A , CM000669.2:g.100626842T>A	GRCh38
NC_000007.13:g.100224465T>A , CM000669.1:g.100224465T>A	GRCh37
NC_000007.12:g.100062401T>A	NCBI36
NG_007989.1:g.19709A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.2057A>T MANE Select	ENSP00000223051.3:p.Glu686Val
ENST00000223051.7:c.2057A>T	ENSP00000223051.3:p.Glu686Val
ENST00000431692.5:c.*732A>T	ENSP00000413905.1:n.*732A>T
ENST00000461176.1:n.403A>T
ENST00000462090.5:n.1093A>T
ENST00000462107.1:c.2057A>T	ENSP00000420525.1:p.Glu686Val
ENST00000465294.5:n.1977A>T
ENST00000476304.5:n.1678A>T
ENST00000490084.5:c.1410A>T
NM_001206855.1:c.1544A>T	NP_001193784.1:p.Glu515Val
NM_003227.3:c.2057A>T	NP_003218.2:p.Glu686Val
XM_005250553.3:c.2057A>T	XP_005250610.1:p.Glu686Val
XM_005250554.3:c.2057A>T	XP_005250611.1:p.Glu686Val
XR_927814.1:n.433+4288T>A
NM_001206855.2:c.1544A>T	NP_001193784.1:p.Glu515Val
XM_005250553.4:c.2057A>T	XP_005250610.1:p.Glu686Val
XM_017012573.1:c.2057A>T	XP_016868062.1:p.Glu686Val
NM_003227.4:c.2057A>T MANE Select	NP_003218.2:p.Glu686Val
NM_001206855.3:c.1544A>T	NP_001193784.1:p.Glu515Val