Canonical Allele Identifier: CA2684106374

Gene: TFR2

Linked Data

• gnomAD v4: 7-100626653-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626654dup , CM000669.2:g.100626654dup	GRCh38
NC_000007.13:g.100224277dup , CM000669.1:g.100224277dup	GRCh37
NC_000007.12:g.100062213dup	NCBI36
NG_007989.1:g.19897dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.2136+109dup MANE Select	ENSP00000223051.3:n.2136+109dup
ENST00000223051.7:c.2136+109dup	ENSP00000223051.3:n.2136+109dup
ENST00000431692.5:c.*811+109dup	ENSP00000413905.1:n.*811+109dup
ENST00000461176.1:n.591dup
ENST00000462090.5:n.1172+109dup
ENST00000462107.1:c.2136+109dup	ENSP00000420525.1:n.2136+109dup
ENST00000465294.5:n.2056+109dup
ENST00000476304.5:n.1757+109dup
ENST00000490084.5:c.1489+109dup
NM_001206855.1:c.1623+109dup	NP_001193784.1:n.1623+109dup
NM_003227.3:c.2136+109dup	NP_003218.2:n.2136+109dup
XM_005250553.3:c.2136+109dup	XP_005250610.1:n.2136+109dup
XM_005250554.3:c.2137-31dup	XP_005250611.1:n.2137-31dup
XR_927814.1:n.433+4100dup
NM_001206855.2:c.1623+109dup	NP_001193784.1:n.1623+109dup
XM_005250553.4:c.2136+109dup	XP_005250610.1:n.2136+109dup
XM_017012573.1:c.2136+109dup	XP_016868062.1:n.2136+109dup
NM_003227.4:c.2136+109dup MANE Select	NP_003218.2:n.2136+109dup
NM_001206855.3:c.1623+109dup	NP_001193784.1:n.1623+109dup