Canonical Allele Identifier: CA368534928

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100231126G>A (hg19) ; chr7:g.100633503G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633503G>A , CM000669.2:g.100633503G>A	GRCh38
NC_000007.13:g.100231126G>A , CM000669.1:g.100231126G>A	GRCh37
NC_000007.12:g.100069062G>A	NCBI36
NG_007989.1:g.13048C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.527C>T MANE Select	ENSP00000223051.3:p.Thr176Ile
ENST00000223051.7:c.527C>T	ENSP00000223051.3:p.Thr176Ile
ENST00000431692.5:c.527C>T	ENSP00000413905.1:p.Thr176Ile
ENST00000462107.1:c.527C>T	ENSP00000420525.1:p.Thr176Ile
ENST00000465294.5:n.532C>T
ENST00000475011.1:n.56C>T
ENST00000476304.5:n.148C>T
NM_001206855.1:c.14C>T	NP_001193784.1:p.Thr5Ile
NM_003227.3:c.527C>T	NP_003218.2:p.Thr176Ile
XM_005250553.3:c.527C>T	XP_005250610.1:p.Thr176Ile
XM_005250554.3:c.527C>T	XP_005250611.1:p.Thr176Ile
NM_001206855.2:c.14C>T	NP_001193784.1:p.Thr5Ile
XM_005250553.4:c.527C>T	XP_005250610.1:p.Thr176Ile
XM_017012573.1:c.527C>T	XP_016868062.1:p.Thr176Ile
NM_003227.4:c.527C>T MANE Select	NP_003218.2:p.Thr176Ile
NM_001206855.3:c.14C>T	NP_001193784.1:p.Thr5Ile