Canonical Allele Identifier: CA2832592542

Gene: TFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633100G= , CM000669.2:g.100633100G=	GRCh38
NC_000007.13:g.100230723G= , CM000669.1:g.100230723G=	GRCh37
NC_000007.12:g.100068659G=	NCBI36
NG_007989.1:g.13451C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.750C= MANE Select	ENSP00000223051.3:p.Tyr250=
ENST00000223051.7:c.750C=	ENSP00000223051.3:p.Tyr250=
ENST00000431692.5:c.750C=	ENSP00000413905.1:p.Tyr250=
ENST00000462107.1:c.750C=	ENSP00000420525.1:p.Tyr250=
ENST00000465294.5:n.755C=
ENST00000473374.5:n.200C=
ENST00000473571.1:n.204C=
ENST00000475011.1:n.279C=
ENST00000476304.5:n.371C=
ENST00000490084.5:c.5C=
NM_001206855.1:c.237C=	NP_001193784.1:p.Tyr79=
NM_003227.3:c.750C=	NP_003218.2:p.Tyr250=
XM_005250553.3:c.750C=	XP_005250610.1:p.Tyr250=
XM_005250554.3:c.750C=	XP_005250611.1:p.Tyr250=
NM_001206855.2:c.237C=	NP_001193784.1:p.Tyr79=
XM_005250553.4:c.750C=	XP_005250610.1:p.Tyr250=
XM_017012573.1:c.750C=	XP_016868062.1:p.Tyr250=
NM_003227.4:c.750C= MANE Select	NP_003218.2:p.Tyr250=
NM_001206855.3:c.237C=	NP_001193784.1:p.Tyr79=