Canonical Allele Identifier: CA020198

Gene: KIF7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89648428G>A , CM000677.2:g.89648428G>A	GRCh38
NC_000015.9:g.90191659G>A , CM000677.1:g.90191659G>A	GRCh37
NC_000015.8:g.87992663G>A	NCBI36
NG_030338.1:g.12024C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.1393C>T	ENSP00000512678.1:p.Arg465Cys
ENST00000394412.8:c.1270C>T MANE Select	ENSP00000377934.3:p.Arg424Cys
ENST00000394412.7:c.1270C>T	ENSP00000377934.3:p.Arg424Cys
NM_198525.2:c.1270C>T	NP_940927.2:p.Arg424Cys
XM_005254902.2:c.1270C>T	XP_005254959.1:p.Arg424Cys
XM_011521531.1:c.1393C>T	XP_011519833.1:p.Arg465Cys
XM_011521532.1:c.1393C>T	XP_011519834.1:p.Arg465Cys
XM_011521533.1:c.1393C>T	XP_011519835.1:p.Arg465Cys
XM_011521534.1:c.1393C>T	XP_011519836.1:p.Arg465Cys
XM_011521535.1:c.1393C>T	XP_011519837.1:p.Arg465Cys
XM_011521536.1:c.1393C>T	XP_011519838.1:p.Arg465Cys
XM_011521537.1:c.1393C>T	XP_011519839.1:p.Arg465Cys
XM_011521531.2:c.1393C>T	XP_011519833.1:p.Arg465Cys
NM_198525.3:c.1270C>T MANE Select	NP_940927.2:p.Arg424Cys