Canonical Allele Identifier: CA2684105707

Gene: TFR2

Linked Data

• gnomAD v4: 7-100620589-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100620589G>T , CM000669.2:g.100620589G>T	GRCh38
NC_000007.13:g.100218212G>T , CM000669.1:g.100218212G>T	GRCh37
NC_000007.12:g.100056148G>T	NCBI36
NG_007989.1:g.25962C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.*268C>A MANE Select	ENSP00000223051.3:n.*268C>A
ENST00000223051.7:c.*268C>A	ENSP00000223051.3:n.*268C>A
ENST00000431692.5:c.*1349C>A	ENSP00000413905.1:n.*1349C>A
ENST00000462090.5:n.1710C>A
ENST00000462107.1:c.*268C>A	ENSP00000420525.1:n.*268C>A
ENST00000465294.5:n.2594C>A
ENST00000476304.5:n.2295C>A
ENST00000490084.5:c.2027C>A
NM_001206855.1:c.*268C>A	NP_001193784.1:n.*268C>A
NM_003227.3:c.*268C>A	NP_003218.2:n.*268C>A
XM_005250553.3:c.*268C>A	XP_005250610.1:n.*268C>A
NM_001206855.2:c.*268C>A	NP_001193784.1:n.*268C>A
XM_005250553.4:c.*268C>A	XP_005250610.1:n.*268C>A
XM_017012573.1:c.*268C>A	XP_016868062.1:n.*268C>A
NM_003227.4:c.*268C>A MANE Select	NP_003218.2:n.*268C>A
NM_001206855.3:c.*268C>A	NP_001193784.1:n.*268C>A