Canonical Allele Identifier: CA2697557469

Gene: TFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633560A>C , CM000669.2:g.100633560A>C	GRCh38
NC_000007.13:g.100231183A>C , CM000669.1:g.100231183A>C	GRCh37
NC_000007.12:g.100069119A>C	NCBI36
NG_007989.1:g.12991T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003227.4:c.474-4T>G MANE Select	NP_003218.2:n.474-4T>G
ENST00000223051.8:c.474-4T>G MANE Select	ENSP00000223051.3:n.474-4T>G
NM_001206855.1:c.-44T>G	NP_001193784.1:n.-44T>G
NM_001206855.2:c.-44T>G	NP_001193784.1:n.-44T>G
NM_001206855.3:c.-44T>G	NP_001193784.1:n.-44T>G
NM_003227.3:c.474-4T>G	NP_003218.2:n.474-4T>G
ENST00000223051.7:c.474-4T>G	ENSP00000223051.3:n.474-4T>G
ENST00000431692.5:c.474-4T>G	ENSP00000413905.1:n.474-4T>G
ENST00000462107.1:c.474-4T>G	ENSP00000420525.1:n.474-4T>G
ENST00000465294.5:n.479-4T>G
ENST00000476304.5:n.91T>G
XM_005250553.3:c.474-4T>G	XP_005250610.1:n.474-4T>G
XM_005250553.4:c.474-4T>G	XP_005250610.1:n.474-4T>G
XM_005250554.3:c.474-4T>G	XP_005250611.1:n.474-4T>G
XM_017012573.1:c.474-4T>G	XP_016868062.1:n.474-4T>G