Canonical Allele Identifier: CA368526416

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100225392T>G (hg19) ; chr7:g.100627769T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100627769T>G , CM000669.2:g.100627769T>G	GRCh38
NC_000007.13:g.100225392T>G , CM000669.1:g.100225392T>G	GRCh37
NC_000007.12:g.100063328T>G	NCBI36
NG_007989.1:g.18782A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.1657A>C MANE Select	ENSP00000223051.3:p.Thr553Pro
ENST00000223051.7:c.1657A>C	ENSP00000223051.3:p.Thr553Pro
ENST00000431692.5:c.*332A>C	ENSP00000413905.1:n.*332A>C
ENST00000462090.5:n.608A>C
ENST00000462107.1:c.1657A>C	ENSP00000420525.1:p.Thr553Pro
ENST00000465294.5:n.1492A>C
ENST00000473374.5:n.730A>C
ENST00000473963.1:n.686A>C
ENST00000476304.5:n.1278A>C
ENST00000490084.5:c.1010A>C
NM_001206855.1:c.1144A>C	NP_001193784.1:p.Thr382Pro
NM_003227.3:c.1657A>C	NP_003218.2:p.Thr553Pro
XM_005250553.3:c.1657A>C	XP_005250610.1:p.Thr553Pro
XM_005250554.3:c.1657A>C	XP_005250611.1:p.Thr553Pro
XR_927814.1:n.434-3387T>G
NM_001206855.2:c.1144A>C	NP_001193784.1:p.Thr382Pro
XM_005250553.4:c.1657A>C	XP_005250610.1:p.Thr553Pro
XM_017012573.1:c.1657A>C	XP_016868062.1:p.Thr553Pro
NM_003227.4:c.1657A>C MANE Select	NP_003218.2:p.Thr553Pro
NM_001206855.3:c.1144A>C	NP_001193784.1:p.Thr382Pro