Canonical Allele Identifier: CA2684105708

Gene: TFR2

Linked Data

• gnomAD v4: 7-100620590-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100620590A>G , CM000669.2:g.100620590A>G	GRCh38
NC_000007.13:g.100218213A>G , CM000669.1:g.100218213A>G	GRCh37
NC_000007.12:g.100056149A>G	NCBI36
NG_007989.1:g.25961T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.*267T>C MANE Select	ENSP00000223051.3:n.*267T>C
ENST00000223051.7:c.*267T>C	ENSP00000223051.3:n.*267T>C
ENST00000431692.5:c.*1348T>C	ENSP00000413905.1:n.*1348T>C
ENST00000462090.5:n.1709T>C
ENST00000462107.1:c.*267T>C	ENSP00000420525.1:n.*267T>C
ENST00000465294.5:n.2593T>C
ENST00000476304.5:n.2294T>C
ENST00000490084.5:c.2026T>C
NM_001206855.1:c.*267T>C	NP_001193784.1:n.*267T>C
NM_003227.3:c.*267T>C	NP_003218.2:n.*267T>C
XM_005250553.3:c.*267T>C	XP_005250610.1:n.*267T>C
NM_001206855.2:c.*267T>C	NP_001193784.1:n.*267T>C
XM_005250553.4:c.*267T>C	XP_005250610.1:n.*267T>C
XM_017012573.1:c.*267T>C	XP_016868062.1:n.*267T>C
NM_003227.4:c.*267T>C MANE Select	NP_003218.2:n.*267T>C
NM_001206855.3:c.*267T>C	NP_001193784.1:n.*267T>C