Canonical Allele Identifier: CA368522080

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100218691A>T (hg19) ; chr7:g.100621068A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100621068A>T , CM000669.2:g.100621068A>T	GRCh38
NC_000007.13:g.100218691A>T , CM000669.1:g.100218691A>T	GRCh37
NC_000007.12:g.100056627A>T	NCBI36
NG_007989.1:g.25483T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.2195T>A MANE Select	ENSP00000223051.3:p.Ile732Asn
ENST00000223051.7:c.2195T>A	ENSP00000223051.3:p.Ile732Asn
ENST00000431692.5:c.*870T>A	ENSP00000413905.1:n.*870T>A
ENST00000462090.5:n.1231T>A
ENST00000462107.1:c.2195T>A	ENSP00000420525.1:p.Ile732Asn
ENST00000465294.5:n.2115T>A
ENST00000476304.5:n.1816T>A
ENST00000490084.5:c.1548T>A
NM_001206855.1:c.1682T>A	NP_001193784.1:p.Ile561Asn
NM_003227.3:c.2195T>A	NP_003218.2:p.Ile732Asn
XM_005250553.3:c.2195T>A	XP_005250610.1:p.Ile732Asn
NM_001206855.2:c.1682T>A	NP_001193784.1:p.Ile561Asn
XM_005250553.4:c.2195T>A	XP_005250610.1:p.Ile732Asn
XM_017012573.1:c.2195T>A	XP_016868062.1:p.Ile732Asn
NM_003227.4:c.2195T>A MANE Select	NP_003218.2:p.Ile732Asn
NM_001206855.3:c.1682T>A	NP_001193784.1:p.Ile561Asn