Canonical Allele Identifier: CA2832592545

Gene: TFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100641198C= , CM000669.2:g.100641198C=	GRCh38
NC_000007.13:g.100238821C= , CM000669.1:g.100238821C=	GRCh37
NC_000007.12:g.100076757C=	NCBI36
NG_007989.1:g.5353G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003227.4:c.64G= MANE Select	NP_003218.2:p.Val22=
ENST00000223051.8:c.64G= MANE Select	ENSP00000223051.3:p.Val22=
NM_003227.3:c.64G=	NP_003218.2:p.Val22=
ENST00000223051.7:c.64G=	ENSP00000223051.3:p.Val22=
ENST00000431692.5:c.64G=	ENSP00000413905.1:p.Val22=
ENST00000462107.1:c.64G=	ENSP00000420525.1:p.Val22=
ENST00000465294.5:n.69G=
ENST00000474947.1:n.222G=
XM_005250553.3:c.64G=	XP_005250610.1:p.Val22=
XM_005250553.4:c.64G=	XP_005250610.1:p.Val22=
XM_005250554.3:c.64G=	XP_005250611.1:p.Val22=
XM_017012573.1:c.64G=	XP_016868062.1:p.Val22=