Canonical Allele Identifier: CA4386224

Gene: TFR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626838C>T , CM000669.2:g.100626838C>T	GRCh38
NC_000007.13:g.100224461C>T , CM000669.1:g.100224461C>T	GRCh37
NC_000007.12:g.100062397C>T	NCBI36
NG_007989.1:g.19713G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.2061G>A MANE Select	ENSP00000223051.3:p.Lys687=
ENST00000223051.7:c.2061G>A	ENSP00000223051.3:p.Lys687=
ENST00000431692.5:c.*736G>A	ENSP00000413905.1:n.*736G>A
ENST00000461176.1:n.407G>A
ENST00000462090.5:n.1097G>A
ENST00000462107.1:c.2061G>A	ENSP00000420525.1:p.Lys687=
ENST00000465294.5:n.1981G>A
ENST00000476304.5:n.1682G>A
ENST00000490084.5:c.1414G>A
NM_001206855.1:c.1548G>A	NP_001193784.1:p.Lys516=
NM_003227.3:c.2061G>A	NP_003218.2:p.Lys687=
XM_005250553.3:c.2061G>A	XP_005250610.1:p.Lys687=
XM_005250554.3:c.2061G>A	XP_005250611.1:p.Lys687=
XR_927814.1:n.433+4284C>T
NM_001206855.2:c.1548G>A	NP_001193784.1:p.Lys516=
XM_005250553.4:c.2061G>A	XP_005250610.1:p.Lys687=
XM_017012573.1:c.2061G>A	XP_016868062.1:p.Lys687=
NM_003227.4:c.2061G>A MANE Select	NP_003218.2:p.Lys687=
NM_001206855.3:c.1548G>A	NP_001193784.1:p.Lys516=