Canonical Allele Identifier: CA368525718

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100225200C>G (hg19) ; chr7:g.100627577C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100627577C>G , CM000669.2:g.100627577C>G	GRCh38
NC_000007.13:g.100225200C>G , CM000669.1:g.100225200C>G	GRCh37
NC_000007.12:g.100063136C>G	NCBI36
NG_007989.1:g.18974G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.1767G>C MANE Select	ENSP00000223051.3:p.Glu589Asp
ENST00000223051.7:c.1767G>C	ENSP00000223051.3:p.Glu589Asp
ENST00000431692.5:c.*442G>C	ENSP00000413905.1:n.*442G>C
ENST00000461176.1:n.28G>C
ENST00000462090.5:n.718G>C
ENST00000462107.1:c.1767G>C	ENSP00000420525.1:p.Glu589Asp
ENST00000465294.5:n.1602G>C
ENST00000473374.5:n.840G>C
ENST00000476304.5:n.1388G>C
ENST00000490084.5:c.1120G>C
NM_001206855.1:c.1254G>C	NP_001193784.1:p.Glu418Asp
NM_003227.3:c.1767G>C	NP_003218.2:p.Glu589Asp
XM_005250553.3:c.1767G>C	XP_005250610.1:p.Glu589Asp
XM_005250554.3:c.1767G>C	XP_005250611.1:p.Glu589Asp
XR_927814.1:n.434-3579C>G
NM_001206855.2:c.1254G>C	NP_001193784.1:p.Glu418Asp
XM_005250553.4:c.1767G>C	XP_005250610.1:p.Glu589Asp
XM_017012573.1:c.1767G>C	XP_016868062.1:p.Glu589Asp
NM_003227.4:c.1767G>C MANE Select	NP_003218.2:p.Glu589Asp
NM_001206855.3:c.1254G>C	NP_001193784.1:p.Glu418Asp