Canonical Allele Identifier: CA368534683

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100231052G>C (hg19) ; chr7:g.100633429G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633429G>C , CM000669.2:g.100633429G>C	GRCh38
NC_000007.13:g.100231052G>C , CM000669.1:g.100231052G>C	GRCh37
NC_000007.12:g.100068988G>C	NCBI36
NG_007989.1:g.13122C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.601C>G MANE Select	ENSP00000223051.3:p.Gln201Glu
ENST00000223051.7:c.601C>G	ENSP00000223051.3:p.Gln201Glu
ENST00000431692.5:c.601C>G	ENSP00000413905.1:p.Gln201Glu
ENST00000462107.1:c.601C>G	ENSP00000420525.1:p.Gln201Glu
ENST00000465294.5:n.606C>G
ENST00000475011.1:n.130C>G
ENST00000476304.5:n.222C>G
NM_001206855.1:c.88C>G	NP_001193784.1:p.Gln30Glu
NM_003227.3:c.601C>G	NP_003218.2:p.Gln201Glu
XM_005250553.3:c.601C>G	XP_005250610.1:p.Gln201Glu
XM_005250554.3:c.601C>G	XP_005250611.1:p.Gln201Glu
NM_001206855.2:c.88C>G	NP_001193784.1:p.Gln30Glu
XM_005250553.4:c.601C>G	XP_005250610.1:p.Gln201Glu
XM_017012573.1:c.601C>G	XP_016868062.1:p.Gln201Glu
NM_003227.4:c.601C>G MANE Select	NP_003218.2:p.Gln201Glu
NM_001206855.3:c.88C>G	NP_001193784.1:p.Gln30Glu