Canonical Allele Identifier: CA651781620

Gene: TFR2

Linked Data

• COSMIC: COSN20888433

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100622391C>T , CM000669.2:g.100622391C>T	GRCh38
NC_000007.13:g.100220014C>T , CM000669.1:g.100220014C>T	GRCh37
NC_000007.12:g.100057950C>T	NCBI36
NG_007989.1:g.24160G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.2137-1265G>A MANE Select	ENSP00000223051.3:n.2137-1265G>A
ENST00000223051.7:c.2137-1265G>A	ENSP00000223051.3:n.2137-1265G>A
ENST00000431692.5:c.*812-1265G>A	ENSP00000413905.1:n.*812-1265G>A
ENST00000462090.5:n.1173-1265G>A
ENST00000462107.1:c.2137-1265G>A	ENSP00000420525.1:n.2137-1265G>A
ENST00000465294.5:n.2057-1265G>A
ENST00000476304.5:n.1758-1265G>A
ENST00000490084.5:c.1490-1265G>A
NM_001206855.1:c.1624-1265G>A	NP_001193784.1:n.1624-1265G>A
NM_003227.3:c.2137-1265G>A	NP_003218.2:n.2137-1265G>A
XM_005250553.3:c.2137-1265G>A	XP_005250610.1:n.2137-1265G>A
XR_927814.1:n.270C>T
NM_001206855.2:c.1624-1265G>A	NP_001193784.1:n.1624-1265G>A
XM_005250553.4:c.2137-1265G>A	XP_005250610.1:n.2137-1265G>A
XM_017012573.1:c.2137-1265G>A	XP_016868062.1:n.2137-1265G>A
NM_003227.4:c.2137-1265G>A MANE Select	NP_003218.2:n.2137-1265G>A
NM_001206855.3:c.1624-1265G>A	NP_001193784.1:n.1624-1265G>A