Canonical Allele Identifier: CA2194727042

Gene: KIF7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89649836T= , CM000677.2:g.89649836T=	GRCh38
NC_000015.9:g.90193067T= , CM000677.1:g.90193067T=	GRCh37
NC_000015.8:g.87994071T=	NCBI36
NG_030338.1:g.10616A=

Transcript Alleles

HGVS	Amino-acid Change
NM_198525.3:c.434A= MANE Select	NP_940927.2:p.Tyr145=
ENST00000394412.8:c.434A= MANE Select	ENSP00000377934.3:p.Tyr145=
NM_198525.2:c.434A=	NP_940927.2:p.Tyr145=
ENST00000394412.7:c.434A=	ENSP00000377934.3:p.Tyr145=
ENST00000445906.1:c.*93A=	ENSP00000395906.1:n.*93A=
ENST00000696512.1:c.557A=	ENSP00000512678.1:p.Tyr186=
XM_005254902.2:c.434A=	XP_005254959.1:p.Tyr145=
XM_011521531.1:c.557A=	XP_011519833.1:p.Tyr186=
XM_011521531.2:c.557A=	XP_011519833.1:p.Tyr186=
XM_011521532.1:c.557A=	XP_011519834.1:p.Tyr186=
XM_011521533.1:c.557A=	XP_011519835.1:p.Tyr186=
XM_011521534.1:c.557A=	XP_011519836.1:p.Tyr186=
XM_011521535.1:c.557A=	XP_011519837.1:p.Tyr186=
XM_011521536.1:c.557A=	XP_011519838.1:p.Tyr186=
XM_011521537.1:c.557A=	XP_011519839.1:p.Tyr186=