Canonical Allele Identifier: CA368523075

Gene: TFR2

Linked Data

• gnomAD v4: 7-100626894-G-T
• MyVariant Identifiers: chr7:g.100224517G>T (hg19) ; chr7:g.100626894G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626894G>T , CM000669.2:g.100626894G>T	GRCh38
NC_000007.13:g.100224517G>T , CM000669.1:g.100224517G>T	GRCh37
NC_000007.12:g.100062453G>T	NCBI36
NG_007989.1:g.19657C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.2005C>A MANE Select	ENSP00000223051.3:p.Leu669Met
ENST00000223051.7:c.2005C>A	ENSP00000223051.3:p.Leu669Met
ENST00000431692.5:c.*680C>A	ENSP00000413905.1:n.*680C>A
ENST00000461176.1:n.351C>A
ENST00000462090.5:n.1041C>A
ENST00000462107.1:c.2005C>A	ENSP00000420525.1:p.Leu669Met
ENST00000465294.5:n.1925C>A
ENST00000476304.5:n.1626C>A
ENST00000490084.5:c.1358C>A
NM_001206855.1:c.1492C>A	NP_001193784.1:p.Leu498Met
NM_003227.3:c.2005C>A	NP_003218.2:p.Leu669Met
XM_005250553.3:c.2005C>A	XP_005250610.1:p.Leu669Met
XM_005250554.3:c.2005C>A	XP_005250611.1:p.Leu669Met
XR_927814.1:n.434-4262G>T
NM_001206855.2:c.1492C>A	NP_001193784.1:p.Leu498Met
XM_005250553.4:c.2005C>A	XP_005250610.1:p.Leu669Met
XM_017012573.1:c.2005C>A	XP_016868062.1:p.Leu669Met
NM_003227.4:c.2005C>A MANE Select	NP_003218.2:p.Leu669Met
NM_001206855.3:c.1492C>A	NP_001193784.1:p.Leu498Met