Canonical Allele Identifier: CA2684105773

Gene: TFR2

Linked Data

• gnomAD v4: 7-100620641-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100620642dup , CM000669.2:g.100620642dup	GRCh38
NC_000007.13:g.100218265dup , CM000669.1:g.100218265dup	GRCh37
NC_000007.12:g.100056201dup	NCBI36
NG_007989.1:g.25909dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.*215dup MANE Select	ENSP00000223051.3:n.*215dup
ENST00000223051.7:c.*215dup	ENSP00000223051.3:n.*215dup
ENST00000431692.5:c.*1296dup	ENSP00000413905.1:n.*1296dup
ENST00000462090.5:n.1657dup
ENST00000462107.1:c.*215dup	ENSP00000420525.1:n.*215dup
ENST00000465294.5:n.2541dup
ENST00000476304.5:n.2242dup
ENST00000490084.5:c.1974dup
NM_001206855.1:c.*215dup	NP_001193784.1:n.*215dup
NM_003227.3:c.*215dup	NP_003218.2:n.*215dup
XM_005250553.3:c.*215dup	XP_005250610.1:n.*215dup
NM_001206855.2:c.*215dup	NP_001193784.1:n.*215dup
XM_005250553.4:c.*215dup	XP_005250610.1:n.*215dup
XM_017012573.1:c.*215dup	XP_016868062.1:n.*215dup
NM_003227.4:c.*215dup MANE Select	NP_003218.2:n.*215dup
NM_001206855.3:c.*215dup	NP_001193784.1:n.*215dup