Canonical Allele Identifier: CA368522776

Gene: TFR2

Linked Data

• dbSNP Id: rs1803267688
• gnomAD v3: 7-100626810-C-T
• gnomAD v4: 7-100626810-C-T
• MyVariant Identifiers: chr7:g.100224433C>T (hg19) ; chr7:g.100626810C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626810C>T , CM000669.2:g.100626810C>T	GRCh38
NC_000007.13:g.100224433C>T , CM000669.1:g.100224433C>T	GRCh37
NC_000007.12:g.100062369C>T	NCBI36
NG_007989.1:g.19741G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.2089G>A MANE Select	ENSP00000223051.3:p.Glu697Lys
ENST00000223051.7:c.2089G>A	ENSP00000223051.3:p.Glu697Lys
ENST00000431692.5:c.*764G>A	ENSP00000413905.1:n.*764G>A
ENST00000461176.1:n.435G>A
ENST00000462090.5:n.1125G>A
ENST00000462107.1:c.2089G>A	ENSP00000420525.1:p.Glu697Lys
ENST00000465294.5:n.2009G>A
ENST00000476304.5:n.1710G>A
ENST00000490084.5:c.1442G>A
NM_001206855.1:c.1576G>A	NP_001193784.1:p.Glu526Lys
NM_003227.3:c.2089G>A	NP_003218.2:p.Glu697Lys
XM_005250553.3:c.2089G>A	XP_005250610.1:p.Glu697Lys
XM_005250554.3:c.2089G>A	XP_005250611.1:p.Glu697Lys
XR_927814.1:n.433+4256C>T
NM_001206855.2:c.1576G>A	NP_001193784.1:p.Glu526Lys
XM_005250553.4:c.2089G>A	XP_005250610.1:p.Glu697Lys
XM_017012573.1:c.2089G>A	XP_016868062.1:p.Glu697Lys
NM_003227.4:c.2089G>A MANE Select	NP_003218.2:p.Glu697Lys
NM_001206855.3:c.1576G>A	NP_001193784.1:p.Glu526Lys