Canonical Allele Identifier: CA1914429257

Gene: RTKN2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62198353T= , CM000672.2:g.62198353T=	GRCh38
NC_000010.10:g.63958112T= , CM000672.1:g.63958112T=	GRCh37
NC_000010.9:g.63628118T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373789.8:c.1385A= MANE Select	ENSP00000362894.3:p.His462=
ENST00000315289.6:c.791A=	ENSP00000325379.2:p.His264=
ENST00000373789.7:c.1385A=	ENSP00000362894.3:p.His462=
NM_145307.3:c.1385A=	NP_660350.2:p.His462=
XM_006717695.2:c.1448A=	XP_006717758.1:p.His483=
XM_011539456.1:c.1490A=	XP_011537758.1:p.His497=
XM_011539457.1:c.1490A=	XP_011537759.1:p.His497=
XM_011539458.1:c.1157A=	XP_011537760.1:p.His386=
XM_011539459.1:c.1448A=	XP_011537761.1:p.His483=
XM_011539460.1:c.1490A=	XP_011537762.1:p.His497=
XM_011539461.1:c.611A=	XP_011537763.1:p.His204=
XM_011539456.2:c.1490A=	XP_011537758.1:p.His497=
XM_011539457.3:c.1490A=	XP_011537759.1:p.His497=
XM_011539460.2:c.1490A=	XP_011537762.1:p.His497=
XM_017015843.1:c.1490A=	XP_016871332.1:p.His497=
XM_017015844.2:c.1385A=	XP_016871333.1:p.His462=
XR_001747053.1:n.1768A=
NM_145307.4:c.1385A= MANE Select	NP_660350.2:p.His462=