Canonical Allele Identifier: CA3005014680

Gene: TFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626738del , CM000669.2:g.100626738del	GRCh38
NC_000007.13:g.100224361del , CM000669.1:g.100224361del	GRCh37
NC_000007.12:g.100062297del	NCBI36
NG_007989.1:g.19813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.2136+25del MANE Select	ENSP00000223051.3:n.2136+25del
ENST00000223051.7:c.2136+25del	ENSP00000223051.3:n.2136+25del
ENST00000431692.5:c.*811+25del	ENSP00000413905.1:n.*811+25del
ENST00000461176.1:n.507del
ENST00000462090.5:n.1172+25del
ENST00000462107.1:c.2136+25del	ENSP00000420525.1:n.2136+25del
ENST00000465294.5:n.2056+25del
ENST00000476304.5:n.1757+25del
ENST00000490084.5:c.1489+25del
NM_001206855.1:c.1623+25del	NP_001193784.1:n.1623+25del
NM_003227.3:c.2136+25del	NP_003218.2:n.2136+25del
XM_005250553.3:c.2136+25del	XP_005250610.1:n.2136+25del
XM_005250554.3:c.2136+25del	XP_005250611.1:n.2136+25del
XR_927814.1:n.433+4184del
NM_001206855.2:c.1623+25del	NP_001193784.1:n.1623+25del
XM_005250553.4:c.2136+25del	XP_005250610.1:n.2136+25del
XM_017012573.1:c.2136+25del	XP_016868062.1:n.2136+25del
NM_003227.4:c.2136+25del MANE Select	NP_003218.2:n.2136+25del
NM_001206855.3:c.1623+25del	NP_001193784.1:n.1623+25del