Canonical Allele Identifier: CA2580775809

Gene: TFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100622225A= , CM000669.2:g.100622225A=	GRCh38
NC_000007.13:g.100219848A= , CM000669.1:g.100219848A=	GRCh37
NC_000007.12:g.100057784A=	NCBI36
NG_007989.1:g.24326T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.2137-1099T= MANE Select	ENSP00000223051.3:n.2137-1099T=
ENST00000223051.7:c.2137-1099T=	ENSP00000223051.3:n.2137-1099T=
ENST00000431692.5:c.*812-1099T=	ENSP00000413905.1:n.*812-1099T=
ENST00000462090.5:n.1173-1099T=
ENST00000462107.1:c.2137-1099T=	ENSP00000420525.1:n.2137-1099T=
ENST00000465294.5:n.2057-1099T=
ENST00000476304.5:n.1758-1099T=
ENST00000490084.5:c.1490-1099T=
NM_001206855.1:c.1624-1099T=	NP_001193784.1:n.1624-1099T=
NM_003227.3:c.2137-1099T=	NP_003218.2:n.2137-1099T=
XM_005250553.3:c.2137-1099T=	XP_005250610.1:n.2137-1099T=
XR_927814.1:n.104A=
NM_001206855.2:c.1624-1099T=	NP_001193784.1:n.1624-1099T=
XM_005250553.4:c.2137-1099T=	XP_005250610.1:n.2137-1099T=
XM_017012573.1:c.2137-1099T=	XP_016868062.1:n.2137-1099T=
NM_003227.4:c.2137-1099T= MANE Select	NP_003218.2:n.2137-1099T=
NM_001206855.3:c.1624-1099T=	NP_001193784.1:n.1624-1099T=