Canonical Allele Identifier: CA2684106382

Gene: TFR2

Linked Data

• gnomAD v4: 7-100626662-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626666dup , CM000669.2:g.100626666dup	GRCh38
NC_000007.13:g.100224289dup , CM000669.1:g.100224289dup	GRCh37
NC_000007.12:g.100062225dup	NCBI36
NG_007989.1:g.19888dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.2136+100dup MANE Select	ENSP00000223051.3:n.2136+100dup
ENST00000223051.7:c.2136+100dup	ENSP00000223051.3:n.2136+100dup
ENST00000431692.5:c.*811+100dup	ENSP00000413905.1:n.*811+100dup
ENST00000461176.1:n.582dup
ENST00000462090.5:n.1172+100dup
ENST00000462107.1:c.2136+100dup	ENSP00000420525.1:n.2136+100dup
ENST00000465294.5:n.2056+100dup
ENST00000476304.5:n.1757+100dup
ENST00000490084.5:c.1489+100dup
NM_001206855.1:c.1623+100dup	NP_001193784.1:n.1623+100dup
NM_003227.3:c.2136+100dup	NP_003218.2:n.2136+100dup
XM_005250553.3:c.2136+100dup	XP_005250610.1:n.2136+100dup
XM_005250554.3:c.2137-40dup	XP_005250611.1:n.2137-40dup
XR_927814.1:n.433+4112dup
NM_001206855.2:c.1623+100dup	NP_001193784.1:n.1623+100dup
XM_005250553.4:c.2136+100dup	XP_005250610.1:n.2136+100dup
XM_017012573.1:c.2136+100dup	XP_016868062.1:n.2136+100dup
NM_003227.4:c.2136+100dup MANE Select	NP_003218.2:n.2136+100dup
NM_001206855.3:c.1623+100dup	NP_001193784.1:n.1623+100dup